Puriderm
FDA Label NDC 51774-005

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Industrias Chamer S.a. De C.v. for the product Puriderm (NDC 51774-005). 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 other, active ingredient, purpose, indications & usage, warnings, otc - keep out of reach of children, otc - stop use, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient

Ethyl Alcohol 70% V/V

Purpose

Antiseptic

Indications & Usage

Apply to hands, skin or any surface twice daily or as often as desired. Not recommendend for wood as it could stain. Don´t spray on or near flame. Avoid contact with eyes. Not for consumption.

Warnings

For external use only. Flammable — Keep away from fire or flame

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.

Otc - Stop Use

  • Stop use and ask a doctor if irritation or redness develops and lasts more than 72 hours.

Other Information

  • Do not store above 105 °F (40 °C).
  • May discolor certain wood surfaces.

Inactive Ingredients

Alcohol Denat, Aqua (Water), Glycerin, Aloe Barbadensis Extract, Phenoxyethanol.

Questions?

M-F: 8-5 CT
+1 781 519-4494

Principal Display Panel - 250 Ml Bottle Label

Puriderm™
ANTIBACTERIAL

MULTI-PURPOSE
SANITIZER
70% ETHYL ALCOHOL

FRAGANCE
FREE

Kills 99.9% of germs and bacteria

WITH ALOE VERA
AND GLYCERIN

SOFT ON THE SKIN

8.4 FL OZ 250 ml

Principal Display Panel (250 ml Bottle Label)

Principal Display Panel (250 ml Bottle Label)

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