Active Ingredient(S)
Ethyl Alcohol 70% v/v.
Hand Sanitizer
FDA Label NDC 74934-030
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 (NDC 74934-030). 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, do not use, otc - when using, otc - stop use, 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
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce germs on the skin.
Warnings
- For external use only.
- Flammable: Keep away from heat or flame.
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Otc - When Using
When using this product: avoid contact with eyes. lf 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: ln case of accidental ingestion, get medical help or contact a poison control center immediately.
Directions
- Squeeze a significant amount in your palm and rub hands until fully dry.
- Rinse free.
Other Information
- Store below 110 °F（43° C).
Inactive Ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl propanol, Aloe Barbadensis leaf Juice, Denatonium benzoate, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Tocopheryl Acetate, Water.
Package Label - Principal Display Panel
59 mL NDC: 74934-030-01
59ml Label (59ml)
1000 mL NDC: 74934-030-02
5000 mL NDC: 74934-030-03
5000ml Label (5000 1)
5000ml Label (5000 2)
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