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

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