Active Ingredient
Ethyl Alcohol 66.5%
Gnc Instant Hand Sanitizer
FDA Label NDC 43655-1111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gnc Holdings Llc for the product Gnc Instant Hand Sanitizer (NDC 43655-1111). 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, uses, warnings, otc - do not use, otc - stop use, 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
Purpose
Antiseptic
Uses
- hand sanitizer to help reduce bacteria on hands and skin
- recommended for repeated use
Warnings
For external use only
Flammable, keep away from fire or flames
Otc - Do Not Use
Do not use in the eyes. If this happens, rinse thoroughly with water
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop and persists
Keep Out Of Reach Of Children
If ingested get medical help or contact a Poison Control Center right away
Directions
- wet hands thoroughly with product
- allow to dry without wiping
- children under 6 should be supervised while using this product
Inactive Ingredients
Purified Water, Carbomer, Aloe Vera, Triethanolamine, Fragrance, D&C Green #5, D&C Yellow #10
Principal Display Panel - 118 Ml Bottle Label
GNC
LIVE WELL
hand
sanitizer
Ethyl Alcohol 66.5%
FRESH SCENT
NDC 43655-1111-0
4.0 FL. OZ. (118 mL)
Principal Display Panel (118 mL Bottle Label)
Principal Display Panel - 237 Ml Bottle Label
GNC
LIVE WELL
hand
sanitizer
Ethyl Alcohol 66.5%
FRESH SCENT
NDC 43655-1111-1
8.0 FL. OZ. (237 mL)
Principal Display Panel (237 mL Bottle Label)
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