FDA.reportPublic FDA data

Underarm Antiperspirant Daily use Charcoal Linen Scent

Manufacturer
Clutch Inc | Wasatch Product Development, LLC.
Effective date
2021-10-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:31:04

Label at a glance#

ProductUnderarm Antiperspirant Daily use Charcoal Linen Scent
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Aluminum Zirconium Tetrachlorohydrex Gly (20%) Antiperspirant

OTC - PURPOSE SECTION

Use

reduces underarm perspiration

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out reach of children. If swallowed get medical help or contact a Poison Control Center right away

INDICATIONS & USAGE SECTION

Stop use if rash or irritation occurs

WARNINGS SECTION

Warnings

For external use only. Do not use on broken skin

DOSAGE & ADMINISTRATION SECTION

DIrections

apply before bed and again in morning

apply to underarm only

INACTIVE INGREDIENT SECTION

Inactive ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Dicaprylyl Carbonate, Fragrance, Hydrogenated Castor Oil, Isopropyl Myristate, Lauryl Methacrylate/Glycol Dimethacrylate Crosspolymer, PEG-8 Distearate, Silica, Propylene Glycol, Ethylhexylglycerin, Maranta Arundinacea Root Extract, Coconut Alkanes, Charcoal Powder, Octenidine Hydrochloride, Coco-Caprylate/Caprate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carpe

Clinical Grade

Underarm

Antiperspirant

Daily Use Charcoal Linen Scent

Net Wt 2 OZ (58 G)

charcoal linencharcoal linen

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74307-00174307-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
SILICON DIOXIDEETJ7Z6XBU4IACT
LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMEREX0F4CZ66HIACT
MARANTA ARUNDINACEA ROOTFVN346W31AIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
PEG-8 DISTEARATE7JNC8VN07MIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
ISOPROPYL ALCOHOLND2M416302IACT
COCONUT ALKANES1E5KJY107TIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
OCTENIDINE HYDROCHLORIDEU84956NU4BIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ACTIVATED CHARCOAL2P3VWU3H10IACT
STEARYL ALCOHOL2KR89I4H1YIACT

Source Document#

Source XML · Source PDF

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
ed75fb5f-a407-59f5-e053-2995a90a9370a3faf8d6-98b5-e627-e053-2a95a90ab5f62022-11-14WarningsExact identifier
spl set id: a3faf8d6-98b5-e627-e053-2a95a90ab5f6

Reported adverse events (FAERS/openFDA)#

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