UNDERARMPLUS ILLUMINATING CITRUS GLOW- aluminum sesquichlorohydrate stick

Drug Labeling and Warnings

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredient

• Active Ingredient: Purpose
• Aluminum Sesquichlorohydrate (15%): Antiperspirant

Uses

Uses

• Reduces underarm perspiration

WARNINGS

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

Directions

Directions

• Apply to underarms only
• Rotate knob to dispense product and rub in vigorously
• Apply every night before bed and again in the morning

INACTIVE INGREDIENT

Inactive Ingredients

Water, C13-14 Isoalkane, Silica, Glyceryl Stearate SE, Cetearyl Alcohol, Silica Silylate, Propylene Glycol, Ethylhexylpalmitate, Zea Mays (Corn) Starch, Ceteareth-20, Hamamelis Virginiana (Witch Hazel) Water, Fragrance, Aminomethyl Propanol, Cocoglycerides, 3-O-Ethyl Ascorbic Acid, Alpha-Arbutin, Sodium Caproyl/Lauroyl Lactylate, Triethyl Citrate, Salvia Officinalis (Sage) Oil, Polysorbate 20, Caprylyl Glycol, Phenoxyethanol

QUESTIONS

Questions:

888-621-0135

help@mycarpe.com

mycarpe.com

Underarm+ Illuminating AP Deo Citrus Glow - 50 g Barrel Label - PDP

Carpe

Underarm+

Illuminating

Antiperspirant Deodorant

Citrus Glow

+Vitamin C Derivative & Alpha Arbutin

NET WT 1.76 oz (50 g)

INGREDIENTS AND APPEARANCE

UNDERARMPLUS ILLUMINATING CITRUS GLOW 
aluminum sesquichlorohydrate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74307-302
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V)	ALUMINUM SESQUICHLOROHYDRATE	15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
WATER (UNII: 059QF0KO0R)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CETEARETH-20 (UNII: YRC528SWUY)
COCOGLYCERIDES (UNII: ISE9I7DNUG)
3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)
SALVIA OFFICINALIS (SAGE) OIL (UNII: U27K0H1H2O)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALPHA-ARBUTIN (UNII: 72VUP07IT5)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
ZEA MAYS (CORN) STARCH (UNII: O8232NY3SJ)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER (UNII: 8FP93ED6H2)
ETHYLHEXYL PALMITATE (UNII: 2865993309)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74307-302-00	50 g in 1 CANISTER; Type 0: Not a Combination Product	05/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	05/01/2026

Labeler - Clutch, Inc (080214892)