BARUBT GLUTA DEODORANT SPARY- gluta deodorant spary spray

BARUBT Gluta Deodorant Spary by

Drug Labeling and Warnings

BARUBT Gluta Deodorant Spary by is a Otc medication manufactured, distributed, or labeled by Guangdong Youbaijia Cosmetic Industry Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ALUMINUM CHLOROHYDRATE 4%
HAMAMELIS VIRGINIANA(WITCH HAZEL)EXTRACT 0.035%
HYDROXYACETOPHENONE 0.005%

INACTIVE INGREDIENT

AQUA
BUTYLENE GLYCOL
HYDROXYETHYLCELLULOSE
PEG-40 HYDROGENATED CASTOR OIL
PRUNUS SPECIOSA FLOWER EXTRACT
GLYCERIN
GLYCERYL GLUCOSIDE
PARFUM
METHYLPARABEN
METHYLISOTHIAZOLINONE
BUTYLENE GLYCOL
1,2-HEXANEDIOL
CAPRYLYL GLYCOL

DO NOT USE

Do not use on damaged skin.

KEEP OUT OF REACH OF CHILDREN

Keep away from children. Do not swallow.

PURPOSE

DEODORANT

QUESTIONS

Contact name: Jessie Peng
Company phone number: +1 818 579 7288
Company e-mail: jessie@registeragentllc.com

STOP USE

lf skin becomes red or irritated, discontinue use immediately and wash with water.

WHEN USING

keep out of eyes. Rinse with water to remove.

STORAGE AND HANDLING

Keep away from light and in adry place.

INDICATIONS & USAGE

STAY FRESH AND CONFIDENT BRIGHTENS UNDERARMS AND PROVIDES LONG-LASTING PROTECTION AGAINSTSWEAT AND ODOR.

WARNINGS

For external use only.

DOSAGE & ADMINISTRATION

CLEAN THE SMELLYPARTS WITH WATER AND WIPETHEM WITH PAPERTOWELS.AT AN ARM'S LENGTH,SPRAY THE ODOROUS AREA ONCE.GENTLY MASSAGE.WAIT FOR 30 SECONDS TO ABSORB INTO FILM.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BARUBT GLUTA DEODORANT SPARY 
gluta deodorant spary spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84712-012
Route of Administration	CUTANEOUS, TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	1.4 g  in 35 mL
HAMAMELIS VIRGINIANA WHOLE (UNII: V663Q8TEFU) (HAMAMELIS VIRGINIANA WHOLE - UNII:V663Q8TEFU)	HAMAMELIS VIRGINIANA WHOLE	0.01225 g  in 35 mL
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) (HYDROXYACETOPHENONE - UNII:G1L3HT4CMH)	HYDROXYACETOPHENONE	0.00175 g  in 35 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	0.0105 g  in 35 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84712-012-01	35 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/13/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	09/13/2024

Labeler - Guangdong Youbaijia Cosmetic Industry Co., Ltd (702314361)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Youbaijia Cosmetic Industry Co., Ltd		702314361	label(84712-012) , manufacture(84712-012)