Over-the-counter drug · OTC MONOGRAPH DRUG
Inon Ace NDC 49873-402
magnesium aluminosilicates, magnesium hydroxide, simethicone · Magnesium hydroxide 60 mg/1 + 2 more ingredients · Tablet · Oral · Sato Pharmaceutical Co., Ltd.
NDC codes
FDA NDC DirectoryProduct NDC (as listed)49873-402Labeler and product segments. Claims need a package NDC.
Product NDC at billing width49873-0402Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 49873-402-01 | 4987304020149873040201 | 1 BOTTLE in 1 CARTON (49873-402-01) / 75 TABLET in 1 BOTTLEMarketed from Nov 1, 1995 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Inon Ace
- Generic name (nonproprietary)
- magnesium aluminosilicates, magnesium hydroxide, simethicone
- Active ingredients
- Magnesium hydroxide — 60 mg/1Silodrate — 200 mg/1Dimethicone — 20 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Sato Pharmaceutical Co., Ltd.NDC labeler code 49873
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 001
- Marketing start
- Listing expires
- Other FDA classes
- Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Skin Barrier Activity (Physiologic effect)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
- Identifiers
- Product ID 49873-402_09d87d9c-fe4c-fd02-e063-6394a90a56bdSPL ID 09d87d9c-fe4c-fd02-e063-6394a90a56bdSPL set ID 0af4355f-e160-409d-8471-2de98dbc6f7cRxCUI 1235450, 1235456UNII NBZ3QY004S, 9T3UU8T0QK, 92RU3N3Y1OUPC 0349873402017
- Pharmacologic class
- Calculi Dissolution Agent; Osmotic Laxative
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N449873040201followed by a unit qualifier and the quantityPackage 49873-0402-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses relieves these symptoms ■heartburn ■acid indigestion ■sour stomach ■upset stomach and gas associated with these symptoms
Excerpt only. Read the full label for complete information.
About NDC 49873-402
- What is NDC 49873-402?
- 49873-402 is the product NDC for Inon Ace, Magnesium hydroxide 60 mg/1 + 2 more ingredients tablet, listed with the FDA by Sato Pharmaceutical Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Inon Ace (Magnesium aluminosilicates, magnesium hydroxide, simethicone).
- What is the active ingredient?
- Magnesium hydroxide, Silodrate, Dimethicone.
- Who is the labeler?
- Sato Pharmaceutical Co., Ltd., NDC labeler code 49873. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Inon Ace?
- 1 other product NDC are listed under this name. See all Inon Ace NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Inon Ace products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Inon Acemagnesium aluminosilicate, magnesium hydroxide | Silodrate 900 mg/30mL; Magnesium hydroxide 250 mg/30mL | SolutionOral | Sato Pharmaceutical Co., Ltd. | 49873-403 | 49873-0403-01 |
Other NDCs under M 001
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Acid Gone Antacidaluminum hydroxide and magnesium carbonate | Aluminum hydroxide 95 mg/15mL; Magnesium carbonate 358 mg/15mL | LiquidOral | Major Pharmaceuticals | 0904-7727 |
| Acid Gone Antacid Extra Strengthaluminum hydroxide and magnesium carbonate | Aluminum hydroxide 160 mg/1; Magnesium carbonate 105 mg/1 | Tablet, ChewableOral | Major Pharmaceuticals | 0904-5365 |
| ADRIAN BICARBONATO SODIUM BICARBONATE USP-4 oz, 8 oz and 16 ozsodium bicarbonate | Sodium bicarbonate 315 mg/g | PowderOral | Evi Labs | 84178-106 |
| Advanced Antacid Mintaluminum hydroxide, magnesium hydroxide, dimethicone | Aluminum hydroxide 400 mg/10mL + 2 more ingredients | SuspensionOral | GOODSENSE | 50804-639 |
| Advanced Regular Strength Antacidaluminum hydroxide, magnesium hydroxide, simethicone | Aluminum hydroxide 200 mg/5mL + 2 more ingredients | SuspensionOral | WALGREEN COMPANY | 0363-1639 |
| Alka-Seltzer Cool Action Extra Strength ReliefChews Mintcalcium carbonate | Calcium carbonate 750 mg/1 | Tablet, ChewableOral | Bayer HealthCare LLC. | 0280-0058 |
| Alka-Seltzer Cool Action Heartburn Relief Mintcalcium carbonate | Calcium carbonate 750 mg/1 | Gum, ChewingOral | Bayer HealthCare LLC. | 0280-0001 |
| Alka-Seltzer Extra Strengthanhydrous citric acid, sodium bicarbonate, and aspirin | Anhydrous citric acid 1000 mg/1 + 2 more ingredients | Granule, EffervescentOral | Bayer HealthCare LLC. | 0280-0211 |
| Alka-Seltzer Extra Strength Heartburn ReliefChewscalcium carbonate | Calcium carbonate 750 mg/1 | Tablet, ChewableOral | Bayer HealthCare LLC. | 0280-0042 |
| Alka-Seltzer Gold | Citric acid monohydrate 1000 mg/1 + 2 more ingredients | Tablet, EffervescentOral | Bayer HealthCare LLC. | 0280-4100 |
| Alka-Seltzer Heartburnanhydrous citric acid, sodium bicarbonate (heat-treated) | Citric acid monohydrate 1000 mg/1; Sodium bicarbonate 1940 mg/1 | Tablet, EffervescentOral | Bayer HealthCare LLC. | 0280-0047 |
| Alka-Seltzer Heartburn Plus Gas ReliefChews Tropical Punchcalcium carbonate and simethicone | Dimethicone 80 mg/1; Calcium carbonate 750 mg/1 | Tablet, ChewableOral | Bayer HealthCare LLC. | 0280-0225 |
| Alka-Seltzer Heartburn Relief Extra Strengthanhydrous citric acid, sodium bicarbonate (heat-treated) | Sodium bicarbonate 1976 mg/1; Citric acid monohydrate 1000 mg/1 | Tablet, EffervescentOral | Bayer Healthcare LLC | 0280-0079 |
| Alka-Seltzer Heartburn Relief Lemon Limeanhydrous citric acid, sodium bicarbonate (heat-treated) | Sodium bicarbonate 1650 mg/1; Citric acid monohydrate 1000 mg/1 | Tablet, EffervescentOral | Bayer Healthcare LLC | 0280-0083 |
| Alka-Seltzer Heartburn Relief Peppermintcalcium carbonate | Calcium carbonate 750 mg/1 | Gum, ChewingOral | Bayer HealthCare LLC. | 0280-0002 |
| Alka-Seltzer Heartburn ReliefChewscalcium carbonate | Calcium carbonate 750 mg/1 | Tablet, ChewableOral | Bayer HealthCare LLC. | 0280-0221 |
| Alka-Seltzer Heartburn ReliefChews Strawberry and Orangecalcium carbonate | Calcium carbonate 750 mg/1 | Tablet, ChewableOral | Bayer HealthCare LLC. | 0280-0224 |
| Alka-Seltzer Kids Tummy ReliefChewscalcium carbonate and dimethicone | Calcium carbonate 750 mg/1; Dimethicone 80 mg/1 | Tablet, ChewableOral | Bayer HealthCare LLC. | 0280-0051 |
| Alka-Seltzer Ultra Strength Heartburn ReliefChewscalcium carbonate | Calcium carbonate 1000 mg/1 | Tablet, ChewableOral | Bayer HealthCare LLC. | 0280-0245 |
| Alka-Seltzer Ultra Strength Heartburn ReliefChews Strawberry and Orangecalcium carbonate | Calcium carbonate 1000 mg/1 | Tablet, ChewableOral | Bayer HealthCare LLC. | 0280-0059 |
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