Puroma
FDA Label NDC 80948-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zenith Micro Control for the product Puroma (NDC 80948-002). 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, warnings, uses, directions, keep out of reach of children., 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  70% V/V

Purpose

Antiseptic.

Warnings

  • Flammable. Keep away from fire or flame.
  • When using this product do not use in or near theeyes. In case of contact, rinse eyes thoroughly with water.
  • Stop use and ask a doctor if irritation or rash appears and lasts.

Uses

Hand Sanitizer to help reduce bacteria on skin.

Directions

  • Put enough product in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using Puroma Hand Sanitizer.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a poison control center right away.

Other Information

  • Store below 110°F (430°C)
  • May discolor certain fabrics or surfaces

Inactive Ingredients

WATER, ISOPROPYL ALCOHOL ,GLYCERIN, ISOPROPYL MYRISTATE,ALPHA.-TOCOPHEROL ACETATE, CARBOMER HOMOPOLYMER , CAPRYLYL GLYCOL,AMINOMETHYLPROPANOL, ALOE VERA LEAF, PROPYLENE GLYCOL,COCO-CAPRYLATE , FRAGRANCE.

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