Active Ingredient
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (15%)
Scentlok Technologies Antiperspirant
FDA Label NDC 69757-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Als Enterprises Inc for the product Scentlok Technologies Antiperspirant (NDC 69757-101). 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 active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
ANTIPERSPIRANT
Use
REDUCES UNDERARM WETNESS
Warnings
- FOR EXTERNAL USE ONLY.
- DO NOT USE ON BROKEN SKIN.
- STOP USE IF RASH DEVELOPS.
- ASK A DOCTOR BEFORE USING IF YOU HAVE KIDNEY DISEASE.
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
MINERAL OIL, CYCLOPENTASILOXANE, STEARYL ALCOHOL, CETYL ALCOHOL, FRAGRANCE/PARFUM, HYDROGENATED CASTOR OIL, GLYCERYL STEARATE, PEG-10 STEARATE, TALC.
Questions?
(800) 315-5799
Package Label.Principal Display Panel
Scentlok_antiperspirant_revised_front (Scentlok Antiperspirant Revised Front)
Scentlok_antiperspirant_revised_back (Scentlok Antiperspirant Revised Back)
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