14% Roll On Anti-Perspirant Deodorant

14% Roll On Anti-Perspirant Deodorant

Drug Labeling and Warnings

Drug Details

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ROLL ON ANTI-PERSPIRANT DEODORANT- aluminum chlorohydrate solution 
Keefe Group

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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14% Roll On Anti-Perspirant Deodorant

Drug Facts

Active ingredient

Aluminum Chlorohydrate, 14% – Anhydrous Basis

Purpose

Antiperspirant

Use

Reduces underarm wetness.

Warnings

For external use only.

Keep out of reach of children.

Do not use on broken skin.

Stop use if rash or irritation occurs.

Ask a doctor before use if you have kidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

Directions

Apply to underarms only.

Inactive ingredients

Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA

Distributed by:
Olivette Products, L.L.C., Bridgeton, MO 63044

PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

FORCE

POWER UP
ANTI-PERSPIRANT
& DEODORANT ROLL-ON

3 fl oz/88 ml

PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

ROLL ON ANTI-PERSPIRANT DEODORANT 
aluminum chlorohydrate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 51870-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE14 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)  
Glycerin (UNII: PDC6A3C0OX)  
Polysorbate 20 (UNII: 7T1F30V5YH)  
Edetate Sodium (UNII: MP1J8420LU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 51870-001-0388 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product06/26/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35006/26/2012
Labeler - Keefe Group (839439601)

Revised: 12/2019
 
Keefe Group


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