Roll On Anti-Perspirant Deodorant

Roll On Anti-Perspirant Deodorant

Drug Labeling and Warnings

Drug Details

k">

ROLL ON ANTI-PERSPIRANT DEODORANT- aluminum chlorohydrate solution 
Bob Barker 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.

----------

Roll On Anti-Perspirant Deodorant

Drug Facts

Active ingredient

Aluminum Chlorohydrate, 10% – 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

PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

Maximum Security

ANTI-PERSPIRANT

& DEODORANT ROLL-ON

1.5 fl oz/45 ml

PRINCIPAL DISPLAY PANEL

ROLL ON ANTI-PERSPIRANT DEODORANT 
aluminum chlorohydrate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 53247-752
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE10 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: 53247-752-0245 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product11/04/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35011/04/2013
Labeler - Bob Barker Inc. (058525536)

Revised: 1/2020
 
Bob Barker Inc.


© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.