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Drug Facts
Dist. by:
COLGATE-PALMOLIVE COMPANY
New York, NY 10022 U.S.A.
Speed Stick Irish Spring Stick
FDA Label NDC 35000-783
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 Speed Stick Irish Spring (NDC 35000-783). 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, 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.
Label Section Quick Index
Active Ingredient
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 13.2%
Purpose
Antiperspirant
Use
reduces underarm wetness
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
Inactive Ingredients
Elaeis Guineensis (Palm) Kernel Oil, Stearyl Alcohol, PPG-14 Butyl Ether, Hydrogenated Castor Oil, C12-15 Alkyl Benzoate, Hydrogenated Soybean Oil, PEG-8 Distearate, Dicaprylyl Ether, Cetyl Alcohol, Behenyl Alcohol, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate, Citric Acid.
Questions?
Call toll-free 1-800-228-7408
Principal Display Panel - 76 G Container Label
SPEED®
STICK
IRISH
SPRING®
ORIGINAL
ANTIPERSPIRANT / DEODORANT
NET WT
2.7 OZ (76 g)
PS0093218
Principal Display Panel (76 g Container Label)
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