Degree Clinical Protection Sheer Powder
FDA Label NDC 64942-1035

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Conopco Inc. D/b/a Unilever for the product Degree Clinical Protection Sheer Powder (NDC 64942-1035). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, warnings, inactive ingredient, otc - questions, otc - do not use, otc - ask doctor, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredient                                                                                Purpose

Aluminum Zirconium Tetrachlorohydrex GLY (20%).................anti-perspirant

Warnings

Warnings    For External Use only

Inactive Ingredient

Cyclopentasiloxane, Dimethicone, Microcrystalline Wax, C18-36 Acid Triglyceride, Fragrance (Parfum), Silica, Zea Mays (Corn) Starch, Dimethicone Crosspolymer, BHT.

Otc - Questions

Questions?  Call toll-free 1-866-DEGREE1

Otc - Do Not Use

Do not use on broken skin

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease

Otc - Stop Use

Stop use if rash or irritation occurs

Otc - Keep Out Of Reach Of Children

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

Package Label.Principal Display Panel

PDP front 1.7oz
PDP 1.7 oz back

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