FDA.reportPublic FDA data

ProCure Antiperspirant and Deodorant

Manufacturer
Twin Med LLC
Effective date
2025-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:07:13

Label at a glance#

ProductProCure Antiperspirant and Deodorant
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure7 sections

Dosage and administration

Directions Apply to underarms only Hold in an upright position about 6 inches from underarm and spray

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Sesquichlorohydrate 15%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Use reduces underarm wetness

Warnings

WARNINGS SECTION

Warnings

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use on broken skin

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if rash or irritation occurs

Ask a doctor before use

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, contact a physician or poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply to underarms only
  • Hold in an upright position about 6 inches from underarm and spray

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Isopropyl Alcohol, Propylene Glycol, Fragrance, PEG 40 Castor Oil, Phenoxyethanol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PCDS04 ImagePCDS04 Image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55681-022-04ProCure Antiperspirant and Deodorant118 mL in 1 BOTTLE, SPRAYSPRAY1181

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55681-02255681-022-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302IACT
PEG-40 CASTOR OIL4ERD2076EFIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ProCure Antiperspirant and DeodorantALUMINUM SESQUICHLOROHYDRATETwin Med LLC39d630ac-86ad-68a1-e063-6394a90a41022025-07-13WarningsExact identifier
ndc (package): 55681-022-04
ndc (product): 55681-022
ndc11 (package): 55681002204
spl id: 39d630ac-86ae-68a1-e063-6394a90a4102
spl set id: 39d630ac-86ad-68a1-e063-6394a90a4102

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.