OTC Medication Information: Axe Signature Island Antiperspirant Deodorant

AXE SIGNATURE ISLAND ANTIPERSPIRANT DEODORANT- 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.

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY(15.2%)

Purpose

antiperspirant

Uses
· reduces underarm wetness

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

Inactive Ingredients Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Fragrance (Parfum), Dimethicone, Polyethylene, Helianthus Annuus (Sunflower) Seed Oil, Steareth-100, BHT.

Questions?

Call toll-free 1-800-450-7580

2.7 oz PDP

.AxeSignatureIslandPDP
(click image for full-size original)

AXE SIGNATURE ISLAND ANTIPERSPIRANT DEODORANT
aluminum zirconium tetrachlorohydrex gly stick
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1420
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Aluminum Zirconium Tetrachlorohydrex GLY (Aluminum Zirconium Tetrachlorohydrex GLY) Aluminum Zirconium Tetrachlorohydrex GLY 15.2 g in 100 g
Inactive Ingredients
Ingredient Name Strength
CYCLOMETHICONE 5
PPG-14 BUTYL ETHER
STEARYL ALCOHOL
HYDROGENATED CASTOR OIL
DIMETHICONE
PEG-8 DISTEARATE
SUNFLOWER OIL
BUTYLATED HYDROXYTOLUENE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:64942-1420-1 76 g in 1 CONTAINER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part350 12/01/2015
Labeler — Conopco Inc. d/b/a Unilever (001375088)
Establishment
Name Address ID/FEI Operations
Unilever Raeford HPCNA 131411576 manufacture (64942-1420)

Revised: 07/2015 Conopco Inc. d/b/a Unilever

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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