What is NDC 17856-5725?

17856-5725 is the product NDC for Mintox Maximum Strength, Aluminum hydroxide 400 mg/5mL + 2 more ingredients suspension, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Mintox Maximum Strength (Aluminum hydroxide, magnesium hydroxide, dimethicone).

What is the active ingredient?

Aluminum hydroxide, Magnesium hydroxide, Dimethicone.

ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Mintox Maximum Strength?

3 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Mintox Maximum Strength NDC 17856-5725

NDC codes

FDA NDC Directory

Product NDC (as listed)17856-5725Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17856-5725Add 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
17856-5725-3	1785657250317856572503	30 mL in 1 CUP (17856-5725-3)Marketed from Jan 28, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Mintox Maximum Strength
Generic name (nonproprietary): aluminum hydroxide, magnesium hydroxide, dimethicone
Active ingredients: Aluminum hydroxide — 400 mg/5mLMagnesium hydroxide — 400 mg/5mLDimethicone — 40 mg/5mL
Dosage form: Suspension
Route: Oral
Labeler: ATLANTIC BIOLOGICALS CORP.NDC labeler code 17856
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M
Marketing start: Feb 1, 2011
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 17856-5725_3b3f429e-d2e4-441c-e063-6294a90aaf4dSPL ID 3b3f429e-d2e4-441c-e063-6294a90aaf4dSPL set ID ac6a47e7-972f-4b82-96da-89926d345e9fRxCUI 237870, 708127UNII 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

N417856572503 followed by a unit qualifier and the quantity

Package 17856-5725-03. 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 Jul 31, 2025.

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 17856-5725

What is NDC 17856-5725?: 17856-5725 is the product NDC for Mintox Maximum Strength, Aluminum hydroxide 400 mg/5mL + 2 more ingredients suspension, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mintox Maximum Strength (Aluminum hydroxide, magnesium hydroxide, dimethicone).
What is the active ingredient?: Aluminum hydroxide, Magnesium hydroxide, Dimethicone.
Who is the labeler?: ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mintox Maximum Strength?: 3 other product NDCs are listed under this name. See all Mintox Maximum Strength NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Mintox Maximum Strength NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Mintox Maximum Strengthaluminum hydroxide, magnesium hydroxide, dimethicone	Aluminum hydroxide 400 mg/5mL + 2 more ingredients	SuspensionOral	MAJOR Pharmaceuticals Inc.	0904-5725	00904-5725-14
Mintox Maximum Strengthaluminum hydroxide, magnesium hydroxide, dimethicone	Aluminum hydroxide 400 mg/5mL + 2 more ingredients	SuspensionOral	NuCare Pharmaceuticals,Inc.	68071-4114	68071-4114-01
Mintox Maximum Strengthaluminum hydroxide, magnesium hydroxide, dimethicone	Aluminum hydroxide 400 mg/5mL + 2 more ingredients	SuspensionOral	Proficient Rx LP	71205-515	71205-0515-35

Other NDCs under M

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

FDA NDC Directory listings under M
Product	Strength	Form · route	Labeler	Product NDC
CETAFEN COUGH and COLDacetaminophen, dextromethorphan hbr, phenylephrine hcl , guaifenesin, ,	Guaifenesin 100 mg/1 + 3 more ingredients	Tablet, Film coatedOral	HART Health	50332-0141
Therastatcherry cough drops	Menthol 5.8 mg/1	LozengeOral	HART Health	50332-0137
Aspirin	Aspirin 325 mg/1	TabletOral	HART Health	50332-0139
MG FoamSan 70ethyl alcohol	Alcohol .7 L/L	LiquidTopical	Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.	50241-223
Cetafen Extraacetaminophen	Acetaminophen 500 mg/1	TabletOral	HART Health	50332-0149
IT Cosmetics Your Skin But Better CC Plus Color Correcting Broad Spectrum SPF 50 Plus Sunscreen Full Coverage Deep Deep Honey Deep Bronze Neutral Deep Deep Mocha Tan Cool Rich Cool Deep Cool Neutral Richhomosalate, octisalate and octocrylene	Homosalate 100 mg/mL + 2 more ingredients	CreamTopical	LOreal USA Products Inc	49967-904
Cetafenacetaminophen	Acetaminophen 325 mg/1	TabletOral	HART Health	50332-0148
MG DermaClean	Benzalkonium chloride .13 g/100g	LiquidTopical	Morgan Gallacher Inc.	50241-014
Antibacterial Liquid Handbenzalkonium chloride	Benzalkonium chloride 13 kg/100kg	LiquidTopical	Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.	50241-317
Relief-PEacetaminophen, phenylephrine, chlorpheniramine	Acetaminophen 325 mg/1 + 2 more ingredients	Tablet, CoatedOral	HART Health	50332-0153
Hand Sanitizer Solution 101benzalkonium chloride	Benzalkonium chloride 13 kg/100kg	LiquidTopical	Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.	50241-224
Histaprindiphenhydramine	Diphenhydramine hydrochloride 25 mg/1	TabletOral	NorMed	50332-0150
MG DermaSan	Benzalkonium chloride .1 g/100g	LiquidTopical	Morgan Gallacher Inc.	50241-259
Nutraloxcalcium carbonate	Calcium carbonate 420 mg/1	Tablet, ChewableOral	HART Health	50332-0151
MG DermaWashbenzalkonium chloride	Benzalkonium chloride 13 kg/100kg	LiquidTopical	Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.	50241-302
Ibuprofen	Ibuprofen 200 mg/1	TabletOral	HART Health	50332-0152
MG DermaGel 62 LVethyl alcohol	Alcohol .62 L/L	LiquidTopical	Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.	50241-464
Eye Cleaneye wash	Water 98.3 mL/100mL	LiquidOphthalmic	HART Health	50332-0201
MG DermaGel 62ethyl alcohol	Alcohol .62 L/L	LiquidTopical	Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.	50241-326
Cetirzacetirizine hcl	Cetirizine hydrochloride 10 mg/1	TabletOral	HART Health	50332-0154

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