Gillette Clinical Protection Cool Wave Clear Gel
FDA Label NDC 69423-584

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Gillette Clinical Protection Cool Wave Clear (NDC 69423-584). 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 other, active ingredient, purpose, use, 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

Other

Drug Facts

For external use only.

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.

Active Ingredient

Aluminum zirconium octachlorohydrex Gly 20% (anhydrous)

Purpose

Antiperspirant

Use

reduces underarm wetness

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.

Directions

  • apply to underarms only
  • apply 3 - 4 clicks of product to underarms at bedtime
  • rub in until clear

Inactive Ingredients

water, cyclopentasiloxane, dimethicone, propylene glycol, alcohol denat., calcium chloride, PEG/PPG-18/18 dimethicone, fragrance

Questions?

1-800-445-5388

* Please review the disclaimer below.