OTC Medication Information: ARRID EXTRA DRY Antiperspirant Deodorant Morning Clean

ARRID EXTRA DRY ANTIPERSPIRANT DEODORANT MORNING CLEAN- aluminum zirconium tetrachlorohydrex gly gel
Church & Dwight Co., Inc.

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 (20%)

Purpose

Antiperspirant

Use

reduces underarm perspiration

Warnings For external use only

Do not use on broken skin

Stop use if rash or irritation occurs

Ask a doctor before use if you have kidney disease

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply a thin layer to underarms only.

Inactive ingredients

Water, SD Alcohol 40, Cyclopentasiloxane, Propylene Glycol, Dimethicone, PEG/PPG-18/18 Dimethicone, Fragrance

Principal Display

MAXIMUM

STRENGTH

PROTECTION

ARRID

EXTRA DRY

CLEAR GEL

ANTIPERSPIRANT

DEODORANT

Morning Clean

NET WT. 2.6 OZ. (73g)

ARLBF-19114-04
(click image for full-size original)
ARRID EXTRA DRY ANTIPERSPIRANT DEODORANT MORNING CLEAN
aluminum zirconium tetrachlorohydrex gly gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:10237-862
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 20 g in 100 g
Inactive Ingredients
Ingredient Name Strength
CYCLOMETHICONE 5
ALCOHOL
PROPYLENE GLYCOL
DIMETHICONE
POLYETHYLENE GLYCOL 900
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:10237-862-28 79 g in 1 CANISTER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part350 09/28/2004
Labeler — Church & Dwight Co., Inc. (001211952)
Establishment
Name Address ID/FEI Operations
Church & Dwight Co., Inc. 043690812 manufacture (10237-862)

Revised: 10/2020 Church & Dwight Co., Inc.

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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