FDA Label for Hand Antiperspirant Nightly Use
View Indications, Usage & Precautions
Hand Antiperspirant Nightly Use Product Label
The following document was submitted to the FDA by the labeler of this product Clutch Inc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredient Purpose
Aluminum Chloride Hexahydrate (15%) Anti-perspirant
Otc - Purpose
Use
- reduces perspiration
Otc - Keep Out Of Reach Of Children
Keep out reach of children. If swallowed get medical help or contact a Poison Control Center right away
Indications & Usage
Stop use and ask a doctor if rash or irritation occurs
Warnings
Warnings
For external use only.
Do not use on broken or irritated skin
Ask a doctor before use if you have kidney disease.
Dosage & Administration
Directions
Wash and dry hands thoroughly before application
Apply a single pump of product to palms each morning
Rub palms together vigorously for 30 seconds
Inactive Ingredient
Inactive Ingredients Aluminum Starch Octenylsuccinate, Aqua (water), Cetyl Hydroxyethylcellulose, Coco-Caprylate/Caprate,Coconut Alkanes, Disodium EDTA, Ethylhexylglycerin, Glycerin, Helianthus Annuus (Suflower) Extract, Hydroxypropyl Starch Phosphate, Octenidine HCL, Oryza Sativa (Rice) Bran Extract, Phenoxyethanol, Polymethylsilsesquioxane, Propanediol, Propylene Glycol, Rosmarinus Officinalis (Rosemary) Leaf Extract, SD Alcohol 40-B, SIlica, Sodium Hydroxide, Tocopherol, Xanthan Gum
Package Label.Principal Display Panel
Carpe
Clinical Grade HAND
Antiperspirant
Nightly Use
15% Aluminum Chloride
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