Anti-Perspirant Deodorant Roll-On Unscented

Anti-Perspirant Deodorant Roll-On Unscented

Drug Labeling and Warnings

Drug Details

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ANTI-PERSPIRANT DEODORANT ROLL-ON  UNSCENTED- aluminum chlorohydrate liquid 
Hydrox Laboratories

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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Anti-Perspirant Deodorant Roll-On Unscented

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. Use daily for best results.

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL - 45 mL Bottle 

Personal Care

Fresh Moment

Anti-Perspirant

Deocorant Roll-On

Alcohol Free

Helps Reduce Wetness

Fragrance Free

Dye Free Formula

Made in USA

NDC: 10565-074-01

MFG BY:
HYDROX LABORATORIES
825-B Tollgate Rd. ∙ Elgin, IL 60123

PRINCIPAL DISPLAY PANEL - 45 mL Bottle Label

ANTI-PERSPIRANT DEODORANT ROLL-ON   UNSCENTED
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 10565-074
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, UNSPECIFIED (UNII: T4V6TWG28D)  
Glycerin (UNII: PDC6A3C0OX)  
Polysorbate 20 (UNII: 7T1F30V5YH)  
EDETATE SODIUM (UNII: MP1J8420LU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 10565-074-0145 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product03/20/2012
2NDC: 10565-074-0259 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product03/20/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35003/20/2012
Labeler - Hydrox Laboratories (025164302)
Registrant - Hydrox Laboratories (025164302)
Establishment
NameAddressID/FEIBusiness Operations
Hydrox Laboratories025164302label(10565-074) , manufacture(10565-074) , pack(10565-074)

Revised: 11/2019
 
Hydrox Laboratories


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