Over-the-counter drug · OTC MONOGRAPH DRUG
Rolaids Ultra Strength 1200 (Calcium carbonate, magnesium hydroxide) NDC 84126-322
Calcium carbonate 1000 mg/1; Magnesium hydroxide 200 mg/1 · Tablet, Chewable · Oral · THE PROCTER & GAMBLE MANUFACTURING COMPANY
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 84126-322-10 | 8412603221084126032210 | 10 TABLET, CHEWABLE in 1 PACKAGE (84126-322-10)Marketed from Dec 6, 2024 | |
| 84126-322-72 | 8412603227284126032272 | 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (84126-322-72)Marketed from Dec 6, 2024 |
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)
- Rolaids Ultra Strength 1200
- Generic name (nonproprietary)
- calcium carbonate, magnesium hydroxide
- Active ingredients
- Calcium carbonate — 1000 mg/1Magnesium hydroxide — 200 mg/1
- Dosage form
- Tablet, Chewable
- Route
- Oral
- Labeler
- THE PROCTER & GAMBLE MANUFACTURING COMPANYNDC labeler code 84126
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 001
- Marketing start
- Listing expires
- Other FDA classes
- Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)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)Phosphate Chelating Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
- Identifiers
- Product ID 84126-322_5cdafd03-d2cb-1d1f-e063-6294a90a7c18SPL ID 5cdafd03-d2cb-1d1f-e063-6294a90a7c18
- Pharmacologic class
- Blood Coagulation Factor; Calculi Dissolution Agent; Osmotic Laxative; Phosphate Binder
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
N484126032210followed by a unit qualifier and the quantityPackage 84126-0322-10. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 84126-322
- What is NDC 84126-322?
- 84126-322 is the product NDC for Rolaids Ultra Strength 1200, Calcium carbonate 1000 mg/1; Magnesium hydroxide 200 mg/1 tablet, chewable, listed with the FDA by THE PROCTER & GAMBLE MANUFACTURING COMPANY. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Rolaids Ultra Strength 1200 (Calcium Carbonate, Magnesium Hydroxide).
- What is the active ingredient?
- Calcium carbonate, Magnesium hydroxide.
- Who is the labeler?
- THE PROCTER & GAMBLE MANUFACTURING COMPANY, NDC labeler code 84126. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Rolaids Ultra Strength 1200?
- 1 other product NDC are listed under this name. See all Rolaids Ultra Strength 1200 NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Rolaids Ultra Strength 1200 products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Rolaids ULTRA STRENGTH 1200calcium carbonate, magnesium hydroxide | Calcium carbonate 1000 mg/1; Magnesium hydroxide 200 mg/1 | Tablet, ChewableOral | THE PROCTER & GAMBLE MANUFACTURING COMPANY | 84126-325 | 84126-0325-1084126-0325-72 |
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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