Active Ingredient(S)
Benzalkonium chloride 0.13%
Hand Sanitizer Towelette
FDA Label NDC 74934-032
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Icolor Biotech Co., Ltd for the product Hand Sanitizer Towelette (NDC 74934-032). 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), purpose, use, warnings, otc - when using, otc - stop 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
Purpose
Antimicrobial
Use
To help reduce microbes on the skin.
Warnings
- For external use only.
- Do not dispose of wipes in flush toilets.
- Flammable: Keep away from fire or flame.
Otc - When Using
When using this product: avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Otc - Stop Use
Stop using and ask a doctor if: irritation or redness develops and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children: in case of accidental ingestion, get medical help or contact a poison control center immediately.
Directions
- No rinsing required, Discard after use.
- Apply to hands or skin.
Other Information
- For external use only.
- Do not dispose of wipes in flush toilets.
- Store below 110° F (43°C)
- May discolor certain fabrics or surfaces.
Inactive Ingredients
Water(Aqua), Methylisothiazolinone, lodopropynyl Butylcarbamate, Glycerol, disodium EDTA, AloeBarbadensisLeafJuice, Tweau, Allantion, RetinylPalmitate, Lanoliue, LsopropylMYRISTATE, Fragrance.
Package Label - Principal Display Panel
1pcs NDC: 74934-032-01
1pcs Label (Wipes 1 1)
1pcs NDC: 74934-032-02
1pcs Label (Wipes 1 2)
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