14% Roll On Anti-Perspirant Deodorant

Roll On Anti-Perspirant Deodorant by

Drug Labeling and Warnings

Roll On Anti-Perspirant Deodorant by is a Otc medication manufactured, distributed, or labeled by New World Imports. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ROLL ON ANTI-PERSPIRANT DEODORANT- aluminum chlorohydrate solution 
New World Imports

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

ROLL ON ANTI-PERSPIRANT DEODORANT 
aluminum chlorohydrate solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51824-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	14 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51824-024-03	88 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	06/22/2012	06/23/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part350	06/22/2012	06/23/2012

Labeler - New World Imports (075372276)

Revised: 12/2019

Document Id: f02537e9-0e5f-4eb9-9828-c6856757f369

34390-5

Set id: d31c7730-6f63-447c-b0c2-ffd7e19a9f01

Version: 3

Effective Time: 20191213