What is NDC 50804-639?

50804-639 is the product NDC for Advanced Antacid Mint, Aluminum hydroxide 400 mg/10mL + 2 more ingredients suspension, listed with the FDA by GOODSENSE. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Advanced Antacid Mint (Aluminum hydroxide, magnesium hydroxide, dimethicone).

What is the active ingredient?

Aluminum hydroxide, Magnesium hydroxide, Dimethicone.

GOODSENSE, NDC labeler code 50804. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Advanced Antacid Mint?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Advanced Antacid Mint NDC 50804-639

NDC codes

FDA NDC Directory

Product NDC (as listed)50804-639Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50804-0639Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
50804-639-12	5080406391250804063912	355 mL in 1 BOTTLE (50804-639-12)Marketed from Jul 1, 2020

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): Advanced Antacid Mint
Generic name (nonproprietary): aluminum hydroxide, magnesium hydroxide, dimethicone
Active ingredients: Aluminum hydroxide — 400 mg/10mLMagnesium hydroxide — 400 mg/10mLDimethicone — 40 mg/10mL
Dosage form: Suspension
Route: Oral
Labeler: GOODSENSENDC labeler code 50804
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 001
Marketing start: Jul 1, 2020
Listing expires: Dec 31, 2026
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 50804-639_0994a3e9-6cf6-8cfc-e063-6394a90a380eSPL ID 0994a3e9-6cf6-8cfc-e063-6394a90a380eSPL set ID a964da1d-e1e3-94a8-e053-2a95a90ac804RxCUI 307746UNII 5QB0T2IUN0, NBZ3QY004S, 92RU3N3Y1O
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

N450804063912 followed by a unit qualifier and the quantity

Package 50804-0639-12. 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 Nov 7, 2023.

Indications (excerpt from the label)

Uses relieves heartburn sour stomach acid indigestion the symptoms referred to as gas

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50804-639

What is NDC 50804-639?: 50804-639 is the product NDC for Advanced Antacid Mint, Aluminum hydroxide 400 mg/10mL + 2 more ingredients suspension, listed with the FDA by GOODSENSE. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Advanced Antacid Mint (Aluminum hydroxide, magnesium hydroxide, dimethicone).
What is the active ingredient?: Aluminum hydroxide, Magnesium hydroxide, Dimethicone.
Who is the labeler?: GOODSENSE, NDC labeler code 50804. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Advanced Antacid Mint?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under M 001

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under M 001
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 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
Alkums antacidcalcium carbonate	Calcium carbonate 500 mg/1	Tablet, ChewableOral	Guardian Drug Company	53041-126

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