Hand Sanitizer (ethyl alcohol) NDC 83986-529

NDC codes

FDA NDC Directory

Product NDC (as listed)83986-529Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83986-0529Add 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
83986-529-16	83986052916	59 mL in 1 BOTTLE, PLASTIC (83986-529-16)Marketed from Dec 22, 2022
83986-529-32	83986052932	355 mL in 1 BOTTLE, PLASTIC (83986-529-32)Marketed from Dec 22, 2022
83986-529-34	83986052934	236 mL in 1 BOTTLE, PLASTIC (83986-529-34)Marketed from Dec 22, 2022
83986-529-86	83986052986	1000 mL in 1 BOTTLE, PLASTIC (83986-529-86)Marketed from Dec 22, 2022

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): Hand Sanitizer
Generic name (nonproprietary): ethyl alcohol
Active ingredients: Alcohol — 70 mL/100mL
Dosage form: Gel
Route: Topical
Labeler: UpLift Brands LLC
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M505G(a)(3)
Marketing start: Dec 22, 2022
Listing expires: Dec 31, 2027
Identifiers: Product ID 83986-529_4cc46e58-b3bd-8b30-e063-6294a90a490bSPL ID 4cc46e58-b3bd-8b30-e063-6294a90a490bSPL set ID dd569334-0280-49d6-afcf-0c49ed316cb9RxCUI 581662UNII 3K9958V90M

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N483986052916 followed by a unit qualifier and the quantity

Package 83986-0529-16. 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 Mar 11, 2026.

Indications (excerpt from the label)

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under M505G(a)(3)

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

FDA NDC Directory listings under M505G(a)(3)
Product	Strength	Form · route	Labeler	Product NDC
Antigingivitis/Antiplaquecetylpyridinium chloride	Cetylpyridinium chloride .7 mg/mL	MouthwashOral	Topco Associates LLC	76162-090
Antigingivitis/Antiplaquecetylpyridinium chloride	Cetylpyridinium chloride .7 mg/mL	MouthwashOral	Meijer, Inc.	79481-0900
Antigingivitis/Antiplaquecetylpyridinium chloride	Cetylpyridinium chloride .5 mg/mL	MouthwashOral	Meijer, Inc.	79481-0953
Antispeticeucalyptol, menthol, methyl salicylate, thymol	Eucalyptol .92 mg/mL + 3 more ingredients	MouthwashOral	Old East Main Co.	55910-664
Antigingivitis/Antiplaquecetylpyridinium chloride	Cetylpyridinium chloride .5 mg/mL	MouthwashOral	Topco Associates LLC	76162-953
b.pure Hand Sanitizer Watermelon Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	FOURSTAR GROUP USA, INC.	80684-124
b.pure Hand Sanitizer Lemon Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	FOURSTAR GROUP USA, INC.	80684-123
b.pure Hand Sanitizer Green Apple Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	FOURSTAR GROUP USA, INC.	80684-125
Antispeticeucalyptol, menthol, methyl salicylate, thymol	Eucalyptol .92 mg/mL + 3 more ingredients	MouthwashOral	Target Corporation	11673-664