Hand Sanitizer
FDA Label NDC 58004-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nationwide Promotions Llc for the product Hand Sanitizer (NDC 58004-001). 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, keep out of reach of children, use, warnings, dosage and administration, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol

Purpose

Antiseptic

Keep Out Of Reach Of Children

If swallowed ,get medical help or contact a Poison on Control Center immediately

Use

Decreases bacteria on hands

Warnings

For external use only
Flammable Keep away from fire or flame
Keep out of eyes In case of eye contact immediaterly flush with water and get medical help

Dosage And Administration

Squeeze on to hands and rub hands  together briskly until dry

Inactive Ingredients

Deionized Water, Carbomer ,Triethanolamine, Aloe barbadensis Gel, Fragrance Glycerin,
Propylene Glycol,Vitamin E

Product Label

Product Label (Label)

Product Label (Label)

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