B-Pure Hand Sanitizer Cherry Scented NDC 80684-203

NDC codes

FDA NDC Directory

Product NDC (as listed)80684-203Labeler and product segments. Claims need a package NDC.

Product NDC at billing width80684-0203Add 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
80684-203-01	80684020301	10 mL in 1 BOTTLE (80684-203-01)Marketed from Mar 12, 2026
80684-203-02	80684020302	59 mL in 1 BOTTLE (80684-203-02)Marketed from Mar 12, 2026

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): B-Pure Hand Sanitizer Cherry Scented
Generic name (nonproprietary): alcohol
Active ingredients: Alcohol — 70 mL/100mL
Dosage form: Liquid
Route: Topical
Labeler: Fourstar Group USA, Inc.
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication 505(a)(3)
Marketing start: Mar 12, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 80684-203_4e08e8dc-b0c7-f4a1-e063-6294a90a45deSPL ID 4e08e8dc-b0c7-f4a1-e063-6294a90a45deSPL set ID 290674c5-1622-451e-abd6-b586117827c3RxCUI 1041849UNII 3K9958V90MUPC 0049696678483, 0049696678490

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

N480684020301 followed by a unit qualifier and the quantity

Package 80684-0203-01. 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 27, 2026.

Indications (excerpt from the label)

Uses hand sanitizer to help reduce bacteria on skin

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 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
Moisturizing Hand Sanitizerethyl alcohol	Alcohol 62 mL/100mL	GelTopical	UpLift Brands, LLC	83986-447
Antispeticeucalyptol, menthol, methyl salicylate, thymol	Eucalyptol .92 mg/mL + 3 more ingredients	MouthwashOral	Valu Merchandisers Company	63941-664