GEM COCONUT VANILLA- aluminum chlorohydrate aerosol, spray

Gem Coconut Vanilla by

Drug Labeling and Warnings

Gem Coconut Vanilla by is a Otc medication manufactured, distributed, or labeled by Gem Products US LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

• ACTIVE INGREDIENTS: PURPOSE
• ALUMINUM CHLOROHYDRATE (20%): ANTIPERSPIRANT

USES

REDUCES UNDERARM WETNESS

WARNINGS

FLAMMABLE. DO NOT USE NEAR HEAT, FLAME OR WHILE SMOKING. CAN CAUSE SERIOUS INJURY OR DEATH.

WHEN USING THIS PRODUCT KEEP AWAY FROM FACE AND MOUTH TO AVOID BREATHING IT. AVOID SPRAYING IN EYES.

CONTENTS UNDER PRESSURE. DO NOT PUNCTURE OR INCINERATE. DO NOT STORE AT TEMPERATURE ABOVE 120°F/50°C OR IN ENCLOSED PLACES THAT COULD OVERHEAT. USE ONLY IN A WELL-VENTILATED AREA.

DO NOT USE ON BROKEN SKIN STOP USE 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 POISON CONTROL CENTER RIGHT AWAY. USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATLY CONCERNTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL.

FOR EXTERNAL USE ONLY

PURPOSE

Antiperspirant

DIRECTIONS

APPLY TO UNDERARMS ONLY. SHAKE WELL. POSITION AROUND 15CM AWAY AND FROM CLEAN, DRY UNDERARMS AND SPRAY. USE EVERYDAY. DO NOT APPLY TO DAMAGED OR SORE SKIN. STOP USE IF IRRITATION DEVELOPS. DO NOT SPRAY NEAR EYES OR FACE.

INACTIVE INGREDIENTS

BUTANE, HYDROFLUOROCARBON 152A, CYCLOPENTASILOXANE, C12-15 ALKYL BENZOATE, ZEA M AYS (CORN) STARCH, WATER (AQUA), FRAGRANCE (PARFUM ), DISTEARDIM ONIUM HECTORITE, TOCOPHERYLACETATE (VITAM IN E), PROPYLENE CARBONATE, BUTYROSPERMUM PARKII (SHEA) BUTTER, CITRIC ACID, PHENOXYETHANOL, SODIUM HYALURONATE (HYALURONICACID).

QUESTIONS ?

CALL + 1-888-203-1463 WWW.GEM-PRODUCTS.CO

PRINCIPAL DISPLAY PANEL

Gem Coconut Vanilla

NET WT. 3.8 oz / 108g / 137ml

INGREDIENTS AND APPEARANCE

GEM COCONUT VANILLA 
aluminum chlorohydrate aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87190-0049
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	20 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
ZEA MAYS (CORN) STARCH (UNII: O8232NY3SJ)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
BUTANE (UNII: 6LV4FOR43R)
HYDROFLUOROCARBON 152A (UNII: 0B1U8K2ME0)
CITRIC ACID (UNII: 2968PHW8QP)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87190-0049-0	108 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/10/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	02/10/2026

Labeler - Gem Products US LLC (144832843)