Sanitizer
FDA Label NDC 76833-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by S Sakhi Corporation for the product Sanitizer (NDC 76833-001). 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 ingridient, purpose, use(s), warnings, directions, keep out of reach of children, inactive ingredient, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingridient

Ethyl Alcohol

Purpose

Antiseptic

Use(S)

For hand sanitizing to reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from fire or flame

Keep out of reach of eyes.

Directions

-Squeeze small amount in your palm and briskly rub hands together until dry.

Keep Out Of Reach Of Children

Keep out of reach of children

Inactive Ingredient

TRIETHANOLAMINE BENZOATE,ALOE VERA LEAF,GLYCERIN,CORBOMER,WATER,FRAGRANCE

Product Label

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