Defense Ag Hand Sanitizer
FDA Label NDC 79930-7105

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nexderma for the product Defense Ag Hand Sanitizer (NDC 79930-7105). 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(s), inactive ingredients, purpose, use, warnings, do not use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient(s)

→ Inactive Ingredients

→ Purpose

→ Use

→ Warnings

→ Do Not Use

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Other Information

→ Package Label - Principal Display Panel

Active Ingredient(S)

Isopropyl Alcohol 75% v/v. Antiseptic to help reduce bacteria that potentially can cause disease

Inactive Ingredients

Ultra Pure Water, Hydroxyethyl Cellulose, Curcumin

Purpose

To help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are unavailable.

Warnings

Keep away form fire and flame.
Flammable
For external use on hands only.
Keep out of eye, ears and mouth.
If contact in eyes, flush thoroughly with water.
Keep out of reach of children.
If swallowed seek medical help immediately or call your poison control center.
Store between 15-30 (58-86F)
Avoid freezing and excessive heat above 40C (104F)
Will damage wood finishes, plastics and some fabrics.