Pure Carnation
FDA Label NDC 42498-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Eng Kah Enterprise Sdn.bhd for the product Pure Carnation (NDC 42498-001). 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[s], warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol 77% v/v.

Purpose

Antiseptic

Use[S]

Health care personnel hand rub used to eliminate infectious germs that can cause diseases immediately and effectively.

Warnings

For external use only...

Flammable. Keep away from heat or flame...

Do not use:

  • In children less than 2 years old.
  • On open skin wound.

    • When using this product keep out eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

Store in cool, dry place (below 300C) and protect from heat. Must put in upright position.

Inactive Ingredients

Water, Glycerin, Carbomer, Fragrance, Punica Granatum Extract, Triethanolamine.

Package Label - Principal Display Panel

Label 2 (Label)

Label 2 (Label)

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