Hand Sanitizer
FDA Label NDC 79882-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Solve Together, Llc for the product Hand Sanitizer (NDC 79882-001). 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 other, active ingredient, purpose, use(s), warnings, do not use, otc - when using, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Other

→ Active Ingredient

→ Purpose

→ Use(s)

→ Warnings

→ Do Not Use

→ Otc - When Using

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Other Information

→ Inactive Ingredients

→ Principal Display Panel - 59 Ml Bottle Label

Other

Drug Facts

DISTRIBUTED BY
TRADEMARK BRAND LLC
1 Bridge Plaza N Ste 475
Fort Lee, NJ 07024

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use(S)

For sanitizing to help reduce bacteria on the skin that potentially can cause disease.

Warnings

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

Do Not Use

With children less than 2 months of age.
On open skin wounds.

Otc - When Using

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children unless under adult supervision. If swallowed, get medical help or contact a poison control center right away.

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.