BABARIA INVISIBLE DEODORANT AND ANTIPERSPIRANT LIQUID ROLL-ON- aluminum chlorohydrate emulsion 
BERIOSKA SL

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Babaria Invisible Deodorant and Antiperspirant Liquid Roll-On

Drug Facts

Active ingredient

Aluminum chlorohydrate 20%

Purpose

Antiperspirant

Uses

Warnings

For external use only

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 mediacal help or contact a Posion Control Center right away.

Directions

Apply to underarms only

Inactive ingredients

Water (aqua), steareth-2, glycerin, steareth-21, niacinamide, ethylhexylglycerin, octenidine HCL, dimethicone, fragrance (parfum), sodium hydroxide, phenoxyethanol, propylene glycol, dehydroacetic acid, benzoic acid, sorbic acid, citronellol, limonene, linalool, alpha-isomethyl ionone.

Package Labeling:

Label07

BABARIA INVISIBLE DEODORANT AND ANTIPERSPIRANT LIQUID ROLL-ON 
aluminum chlorohydrate emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78283-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE200 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
STEARETH-2 (UNII: V56DFE46J5)  
GLYCERIN (UNII: PDC6A3C0OX)  
STEARETH-21 (UNII: 53J3F32P58)  
NIACINAMIDE (UNII: 25X51I8RD4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
SORBIC ACID (UNII: X045WJ989B)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78283-004-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product03/18/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01903/18/2024
Labeler - BERIOSKA SL (462392556)

Revised: 12/2023
Document Id: 0cf5c07f-8c88-2ee6-e063-6394a90a893d
Set id: 7e6dffe7-4554-4b55-91b5-9d45bbd97913
Version: 1
Effective Time: 20231220
 
BERIOSKA SL