FDA Label for Hcs Roll-on Antiperspirant
View Indications, Usage & Precautions
Hcs Roll-on Antiperspirant Product Label
The following document was submitted to the FDA by the labeler of this product Concordance Healthcare Solutions, Llc.. 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.
Active Ingredient
Aluminum Chlorohydrate 4.5%
Purpose
Antiperspirant
Use
Reduces underarm perspiration.
Warnings
For external use only
Otc - Do Not Use
Do not use on broken skin. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
Otc - Ask Doctor
Ask a doctor before use if you have kidney disease.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help and contact Poison Control Center right away.
Directions
Apply to underarms only.
Inactive Ingredients
Ceteareth-24. Cetearyl Alcohol, Fragrance, Isopropyl Palmitate, Magnesium Aluminum Silicate, Methylparaben, Paraffinum Liquidum, Propylparaben, Sodium Benzoate, Water
Principal Display Panel – 44 Ml Bottle, Dispensing Label
HCS
NDC 83506-004-01
Clean Fresh Scent
Roll-On
Antiperspirant/
Deodorant
- Fights Wetness & Odor
1.5 FL. OZ. (44ml)
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