ANTIPERSPIRANT DRY 1.6 OZ LADY ANTIPERSPIRANT- aluminum chlorohydrate aerosol, spray 
Rejoice International Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Antiperspirant Dry 1.6 oz Lady

Active Ingredient ........................................................................... Purpose

Aluminum Chlorohydrate 23.3% .................................................. Antiperspirant

Antiperspirant

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reduces underarm wetness

Warnings

For external use only.

Flammable.

Do not spray near flame or while smoking.
Contents under pressure
Do not crush, puncture or incinerate container.
Do not expose to heat or store at temperatures above 120oF
Do not use on broken skin.
Ask a doctor before using, if you have kidney disease.
When using this product
Keep away from face and mouth to avoid breathing it. Avoid spraying in eyes.
Use only directed. Intentional missuse by deliberately concentrating and inhaling the contents can be harmful or fatal
Stop use if rash or irritation develops.

Directions

Inactive Ingredients

Isobutane, Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Ethyl Alcohol, PPG-14 Butyl Ether, Helianthus Annuus Seed Oil, Isopropryl Myristate, C12-15 Alkyl Benzoate, Frangrance, Propane, Aluminum Starch Ocetenylsuccinate, Disteardimonium Hectorite, Dimethicone, Tocopheryl Acetate, BHT, Silica

label

ANTIPERSPIRANT DRY 1.6 OZ LADY  ANTIPERSPIRANT
aluminum chlorohydrate aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57337-106
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE23.3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
ALCOHOL (UNII: 3K9958V90M)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
ISOBUTANE (UNII: BXR49TP611)  
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
PROPANE (UNII: T75W9911L6)  
LAURYL PHOSPHATE (UNII: 0K08L8GE2H)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57337-106-0145 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35001/13/2020
Labeler - Rejoice International Inc. (078741245)
Establishment
NameAddressID/FEIBusiness Operations
Sanit & Sons Company Limited660220096manufacture(57337-106)

Revised: 1/2020
Document Id: 9c0d8c82-6c4d-a511-e053-2995a90a793f
Set id: 9c0d5f62-a757-7ab7-e053-2995a90a47d9
Version: 1
Effective Time: 20200113
 
Rejoice International Inc.