OTC Medication Information: Dry Idea Antiperspirant

DRY IDEA ANTIPERSPIRANT- aluminum zirconium octachlorohydrex gly gel
Henkel Corporation

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 Octachlorohydrex GLY 16.4%

Purpose

Antiperspirant

Use

• Reduces underarm perspiration • Extra effective

Warnings

For external use only. Do not use on broken skin.

Stop use and ask a doctor

if rash or irritation occurs.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away.

Ask a doctor before use if

you have kidney disease.

Directions

Apply to underarms only.

Inactive Ingredients

Aqua (Water, Eau) • Aluminum Zirconium Octachlorohydrex GLY • Alcohol Denat. • Cyclomethicone • Propylene Glycol • Dimethicone • Calcium Chloride • Trisiloxane • PEG/PPG-18/18 Dimethicone • TButyl Alcohol

Do not freeze or store above 105⁰F

Questions? 1-800-258-DIAL

54340-291-54 (3oz -- 1970545 FL)
(click image for full-size original)

54340-291-54 (3oz -- 1970546 BL)
(click image for full-size original)
DRY IDEA ANTIPERSPIRANT
dry idea clear gel antiperspirant — powder fresh gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-291
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY) ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY 16.4 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER 46.9 g in 100 g
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:54340-291-54 85 g in 1 CANISTER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part350 01/01/2015
Labeler — Henkel Corporation (080887708)
Registrant — Henkel Corporation (080887708)
Establishment
Name Address ID/FEI Operations
VVF ILLINOIS SERVICES LLC 024177178 manufacture (54340-291)

Revised: 02/2020 Henkel Corporation

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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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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