Lady Speed Stick
FDA Label NDC 35000-855

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Colgate Palmolive Company for the product Lady Speed Stick (NDC 35000-855). 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, uses, warnings, otc - do not use, otc - ask doctor, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

Drug Facts

Dist. by:
COLGATE-PALMOLIVE COMPANY
New York, NY 10022

Active Ingredient

Aluminum zirconium tetrachlorohydrex gly 18%

Purpose

Antiperspirant

Uses

  • reduces underarm wetness
  • lasts all day

Warnings

For external use only

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
  • turn dial to raise product

Inactive Ingredients

water, cyclomethicone, SD alcohol 40-B, tripropylene glycol, dimethicone, propylene glycol, phenyl trimethicone, fragrance, PEG/PPG-18/18 dimethicone

Questions?

Call toll-free 1-800-228-7408

Principal Display Panel - 65 G Container Label

fresh
fusion®

lady
Speed
Stick
®

24/7
WETNESS & ODOR PROTECTION
GEL

antiperspirant/deodorant
NET WT 2.3 OZ (65 g)

Principal Display Panel (65 g Container Label)

Principal Display Panel (65 g Container Label)

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