Hcs Roll-on Antiperspirant Liquid
FDA Label NDC 83506-004

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Concordance Healthcare Solutions, Llc. for the product Hcs Roll-on Antiperspirant (NDC 83506-004). 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 - do not use, otc - ask doctor, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

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)

    Principal Display Panel – 44 mL Bottle, Dispensing Label (Hcs03 0000 01)

    Principal Display Panel – 44 mL Bottle, Dispensing Label (Hcs03 0000 01)

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