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Antiperspirant Wipe

XERO Antiperspirant Wipe

Approved
Approval ID

326c944a-8beb-d33d-e063-6294a90ae2a9

Product Type

HUMAN OTC DRUG LABEL

Effective Date

Apr 22, 2025

Manufacturers
FDA

Stock Your Home

DUNS: 024652770

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Aluminum Chlorohydrate

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code85505-395
Application NumberM019
Product Classification
M
Marketing Category
C200263
G
Generic Name
Aluminum Chlorohydrate
Product Specifications
Route of AdministrationTOPICAL
Effective DateApril 22, 2025
FDA Product Classification

INGREDIENTS (14)

POLYSORBATE 20Inactive
Code: 7T1F30V5YH
Classification: IACT
ALUMINUM CHLOROHYDRATEActive
Quantity: 15 g in 100 1
Code: HPN8MZW13M
Classification: ACTIB
PHENOXYETHANOLInactive
Code: HIE492ZZ3T
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SORBIC ACIDInactive
Code: X045WJ989B
Classification: IACT
PEG-180Inactive
Code: Q662QK8M3B
Classification: IACT
.ALPHA.-TOCOPHEROL ACETATEInactive
Code: 9E8X80D2L0
Classification: IACT
TOCOPHEROLInactive
Code: R0ZB2556P8
Classification: IACT
USNEA BARBATAInactive
Code: D6DVA9TCAP
Classification: IACT
CHLORPHENESINInactive
Code: I670DAL4SZ
Classification: IACT
POTASSIUM SORBATEInactive
Code: 1VPU26JZZ4
Classification: IACT
SAGEInactive
Code: 065C5D077J
Classification: IACT
BENZYL ALCOHOLInactive
Code: LKG8494WBH
Classification: IACT
BENZOIC ACIDInactive
Code: 8SKN0B0MIM
Classification: IACT

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Antiperspirant Wipe - FDA Drug Approval Details