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Anti-Perspirant Deodorant Roll-On Unscented

Dosage form: liquid
Ingredients: Aluminum Chlorohydrate 10mg in 100mL
Labeler: Hydrox Laboratories
NDC Code: 10565-074

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.

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

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

PRINCIPAL DISPLAY PANEL - 45 mL Bottle Label

Personal Care

FreshMoment

Anti-Perspirant
Deodorant Roll-On
Alcohol-Free

Helps Reduce Wetness
FRAGRANCE FREE
Dye Free Formula

MADE IN USA

1.5 FL. OZ. (45mL)

ANTI-PERSPIRANT DEODORANT ROLL-ON   UNSCENTED
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10565-074
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum Chlorohydrate (Aluminum Chlorohydrate) Aluminum Chlorohydrate10 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Hydroxyethyl Cellulose (2000 MPA.S at 1%) 
Glycerin 
Polysorbate 20 
Edetate Sodium 
Packaging
#Item CodePackage Description
1NDC:10565-074-0145 mL in 1 BOTTLE, WITH APPLICATOR
2NDC:10565-074-0259 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35003/20/2012
Labeler - Hydrox Laboratories (025164302)
Establishment
NameAddressID/FEIOperations
Hydrox Laboratories025164302MANUFACTURE(10565-074)

Revised: 03/2012
Document Id: a9e2c89a-f6d6-4632-9609-36cdb007c47b
Set id: a3454d37-ded4-40db-a6b4-c56255796fca
Version: 1
Effective Time: 20120321
 
Hydrox Laboratories

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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