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Name:Axe Dry Phoenix
Manufacturer:Conopco Inc. D/b/a Unilever
Category:Over-the-counter (OTC) Marketed Drugs


Axe Dry Phoenix Antiperspirant Deodorant

AXE  DRY PHOENIX - aluminum zirconium tetrachlorohydrex gly stick 
Conopco Inc. d/b/a Unilever

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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Axe Dry Phoenix Antiperspirant Deodorant

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY(18.2%)

Purpose
anti-perspirant

Uses
· reduces underarm wetness
· 24 hour protection

Warnings
For external use only

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irritation occurs

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions
·
apply to underarms only
· turn dial to raise product
· to ensure product appears clear on skin, do not overapply
· replace cap

Inactive ingredients

Cyclopentasiloxane, PPG-14 Butyl Ether, Stearyl Alcohol, Hydrogenated Castor Oil, PEG-8 Distearate, Talc, Fragrance (Parfum), BHT

Questions?

Call toll-free 1-800-450-7580

Phoenix 2.7 oz PDP
Axe Dry Phoenix 2.7 PDP

AXE   DRY PHOENIX
aluminum zirconium tetrachlorohydrex gly stick
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1164
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Aluminum Zirconium Tetrachlorohydrex GLY (Aluminum cation) Aluminum Zirconium Tetrachlorohydrex GLY 18.2 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
CYCLOMETHICONE 5  
PPG-14 BUTYL ETHER  
STEARYL ALCOHOL  
HYDROGENATED CASTOR OIL  
PEG-8 DISTEARATE  
TALC  
BUTYLATED HYDROXYTOLUENE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:64942-1164-1 76 g in 1 CONTAINER None
2 NDC:64942-1164-2 48 g in 1 CONTAINER None
3 NDC:64942-1164-3 14 g in 1 CONTAINER None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part350 06/01/2011

Labeler - Conopco Inc. d/b/a Unilever (001375088)
Establishment
Name Address ID/FEI Operations
Unilever Raeford HPCNA 131411576 manufacture

Revised: 06/2011 Conopco Inc. d/b/a Unilever



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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