CARPE ANTIPERSPIRANT COCONUT VANILLA- aluminum. sesquichlorohydrate stick

Carpe Antiperspirant Coconut Vanilla by

Drug Labeling and Warnings

Carpe Antiperspirant Coconut Vanilla by is a Otc medication manufactured, distributed, or labeled by Clutch Inc, Derma Care Research Labss, LLC, Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Aluminum Sesquichlorohydrate 20%

PURPOSE

Anti-perspirant

INDICATIONS & USAGE

Reduces underarm perspiration.

WARNINGS

For external use only.

Do not use on broken or irritated skin

Stop use and ask a doctor if rash or irritation occurs

Ask a doctor before use if you have kidney disease

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Apply to underarms only

Rotate knob to dispense product and rub in vigorously

Apply every night before going to bed and again in the morning

INACTIVE INGREDIENT

Water, C13-14 Isoalkane, Silica, Cetearyl Alcohol, Glyceryl Monostearate SE, Silica Silylate, Ethyhexyl Palmitate, Propylene Glycol, Zea Mays (Corn) Starch, Aminomethyl Propanol, Ceteareth-20, Hamamelis Virginiana (Witch Hazel) Water, Fragrance, Coco Glycerides, Salvia Officinalis (Sage) Oil, Sodium Caproyl/Lauroyl Lactylate, Triethyl Citrate, Phenoxyethanol, Alcohol, Caprylyl Glycol, Polysorbate 20

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CARPE ANTIPERSPIRANT COCONUT VANILLA 
aluminum. sesquichlorohydrate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74307-825
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V)	ALUMINUM SESQUICHLOROHYDRATE	20 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
SODIUM CAPROYL LACTYLATE (UNII: 87WR3BHC09)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SILICA (UNII: ETJ7Z6XBU4)
CETEARETH-20 (UNII: YRC528SWUY)
SAGE OIL (UNII: U27K0H1H2O)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
COCOGLYCERIDES (UNII: ISE9I7DNUG)
ZEA MAYS (CORN) STARCH (UNII: O8232NY3SJ)
WATER (UNII: 059QF0KO0R)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74307-825-01	50 g in 1 CONTAINER; Type 0: Not a Combination Product	04/29/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	04/29/2025

Labeler - Clutch Inc (080214892)

Registrant - Derma Care Research Labss, LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(74307-825)