Antiperspirant Wipe for Women NDC 71592-001

NDC codes

FDA NDC Directory

Product NDC (as listed)71592-001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71592-0001Add 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
71592-001-86	71592000186	6 PACKET in 1 PACKAGE (71592-001-86) / 3 g in 1 PACKET (71592-001-85)Marketed from Jul 18, 2017

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): Antiperspirant Wipe for Women
Generic name (nonproprietary): aluminum chlorohydrate
Active ingredients: Aluminum chlorohydrate — 15 g/100g
Dosage form: Swab
Route: Topical
Labeler: FlawlessWipes, LLC
Product type: Over-the-counter drug
Marketing category: OTC monograph (final)Application part350
Marketing start: Jul 18, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 71592-001_6148c5e0-d631-4d8d-8972-123bedffff66SPL ID 6148c5e0-d631-4d8d-8972-123bedffff66SPL set ID a94d0d85-2537-424f-87c8-6aeade047800UNII HPN8MZW13MUPC 0040232376603

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

N471592000186 followed by a unit qualifier and the quantity

Package 71592-0001-86. 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 17, 2017.

Indications (excerpt from the label)

USES Underarm antiperspirant to reduce perspiration and odor

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under part350

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

FDA NDC Directory listings under part350
Product	Strength	Form · route	Labeler	Product NDC
Mitchum Advance Control Pure Freshaluminum chlorohydrate	Aluminum chlorohydrate .25 g/mL	AerosolTopical	Revlon Consumer Products Corp	10967-649
Mitchum Advance Controlaluminum chlorohydrate	Aluminum chlorohydrate .25 g/mL	AerosolTopical	Revlon Consumer Products Corp	10967-635
Mitchum Advance Control Sportaluminum chlorohydrate	Aluminum chlorohydrate .25 g/mL	AerosolTopical	Revlon Consumer Products Corp	10967-636
Mitchum Advance Control Powder Freshaluminum chlorohydrate	Aluminum chlorohydrate .25 g/mL	AerosolTopical	Revlon Consumer Products Corp	10967-637
Mitchum Advance Controlaluminum chlorohydrate	Aluminum chlorohydrate .25 g/mL	AerosolTopical	Revlon Consumer Products Corp	10967-638

Antiperspirant Wipe for Women (aluminum chlorohydrate) NDC 71592-001