Moisturizing Hand Sanitizer (ethyl alcohol) NDC 83986-447

NDC codes

FDA NDC Directory

Product NDC (as listed)83986-447Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83986-0447Add 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
83986-447-45	83986044745	1150 mL in 1 BOTTLE, PLASTIC (83986-447-45)Marketed from Apr 12, 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): Moisturizing Hand Sanitizer
Generic name (nonproprietary): ethyl alcohol
Active ingredients: Alcohol — 62 mL/100mL
Dosage form: Gel
Route: Topical
Labeler: UpLift Brands, LLC
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication 505(a)(3)
Marketing start: Apr 12, 2024
Listing expires: Dec 31, 2027
Identifiers: Product ID 83986-447_4cc43159-6f6b-223d-e063-6294a90a6d6dSPL ID 4cc43159-6f6b-223d-e063-6294a90a6d6dSPL set ID a1954926-35f6-439e-863f-29351013e554UNII 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

N483986044745 followed by a unit qualifier and the quantity

Package 83986-0447-45. 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 505(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 505(a)(3)
Product	Strength	Form · route	Labeler	Product NDC
B-Pure Hand Sanitizer Fig Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	Fourstar Group USA, Inc.	80684-204
B-Pure Hand Sanitizer Cherry Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	Fourstar Group USA, Inc.	80684-203
Antispeticeucalyptol, menthol, methyl salicylate, thymol	Eucalyptol .92 mg/mL + 3 more ingredients	MouthwashOral	Valu Merchandisers Company	63941-664
B-Pure Hand Sanitizer Vanilla Honey Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	Fourstar Group USA, Inc.	80684-205
B-Pure Moisturizing Hand Sanitizer Peachy Cherry Bliss Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	Fourstar Group USA, Inc.	80684-206
B-Pure Moisturizing Hand SanitizerSugared Strawberry Scentedalcohol	Alcohol 70 mL/100mL	LiquidTopical	Fourstar Group USA, Inc.	80684-207