Golden Grooming Company Hand Sanitizer
FDA Label NDC 73834-202

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Square M Llc for the product Golden Grooming Company Hand Sanitizer (NDC 73834-202). 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 drug facts, active ingredient(s), purpose, warning, directions, other information, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient(S)

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Warning

For external use only. Flammable. Keep away from heat or flame

Do not use:

■ in children less than 2 months of age

■ on open skin wounds

When using this product keep out of 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.

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 between 15-30C (59-86F)

■ Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

water, glycerin, PEG-6 (AND) AMP-acrylates/vinyl isodecanoate crosspolymer, aloe barbadensis (aloe vera) leaf juice, tocopheryl acetate (vitamin E acetate)

Packaging

Image (7383420216(1))

Image (7383420216(1))

Image (7383420216(2))

Image (7383420216(2))

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