Anti-Perspirant Deodorant Spray

Anti-Perspirant Deodorant Spray

Drug Labeling and Warnings

Drug Details

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ANTI-PERSPIRANT DEODORANT- aluminum chlorohydrate spray 
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 Spray

Drug Facts

Active ingredient

Aluminum Chlorohydrate, 13% - 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

Hold two inches from underarm and spray. Use daily for best results.

Inactive ingredients

Purified Water, Isopropyl Alcohol, Propylene Glycol, Peg-40 Hydrogenated Castor Oil, Fragrance.

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

PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label

Personal Care

FreshMoment

Anti-Perspirant
Deodorant Spray

Helps Reduce Wetness
Spring Fresh Fragrance

MADE IN USA

2 FL. OZ. (59mL)

Principal Display Panel - 59 ml Bottle Label
ANTI-PERSPIRANT DEODORANT 
aluminum chlorohydrate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 10565-067
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE13 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Isopropyl Alcohol (UNII: ND2M416302)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Polyoxyl 40 Hydrogenated Castor Oil (UNII: 7YC686GQ8F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 10565-067-0259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/11/2011
2NDC: 10565-067-04118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/11/201101/02/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35011/11/2011
Labeler - Hydrox Laboratories (025164302)
Registrant - Hydrox Laboratories (025164302)
Establishment
NameAddressID/FEIBusiness Operations
Hydrox Laboratories025164302MANUFACTURE(10565-067) , label(10565-067) , pack(10565-067)

Revised: 10/2019
 
Hydrox Laboratories


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