Otc - Active Ingredient
Aluminum Zirconium Tetrachlorohydren GLY (18%)
Helmm Antiperspirant Deodorant Hudson Gel
FDA Label NDC 72147-1801
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zgtl, Llc for the product Helmm Antiperspirant Deodorant Hudson (NDC 72147-1801). 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, inactive ingredient, indications & usage, warnings, otc - keep out of reach of children, otc - purpose, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Cetyl Alcohol, C12-C15 Alkyl Benzoate, Dimethicone 10 CST, Hydrogenated Castor Oil, Behenyl Alcohol, Sunflower Seed Oil, Vegetable Glycerin, Tapioca Starch, Steareth-2, Corn Starch, Fragrance, Vitamin E Acetate, Aloe Leaf Extract
Indications & Usage
Uses: reduces underarm wetness
Warnings
Warnings
For external use only
Do not use on broken skin
Ask a doctor before use if you have kidney disease
Stop use if rash or irritation occurs
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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.
Otc - Purpose
Uses: reduces underarm wetness​
Package Label.Principal Display Panel
Hudson (Hudson)
* Please review the disclaimer below.
