Other
NA
Grand Innovations Hand Sanitizer
FDA Label NDC 74765-011
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 Yiwu Limei Cosmetics Co., Ltd for the product Grand Innovations Hand Sanitizer (NDC 74765-011). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient(S)
Ethyl Alcohol 70% v/v. Purpose: Antiseptic
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help decrease bacteria on skin. when water, soap& towel are not available. recommended for repeated use.
Warnings
For external use only: hands. Flammable. Keep away from fire or flame
Do Not Use
- Do not apply around eyes.Do not use in ears&mouth
Otc - When Using
When using this product avoid contact with eyes, In case of contact flush eyes with water.
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.
Keep out of reach of children. Children must be supervised in use of this product.
Otc - Stop Use
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be supervised in use of this product.
Directions
wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision,
not recommended for infants
Other Information
store between 59-86F (15~30C) ,may discolor some fabrics， harmful to wood finishes and plastics
Inactive Ingredients
water, propylene glycol,glycerin, carbomer.triethanolamine
Package Label - Principal Display Panel
50 mL NDC: 74765-011-01
50ml Label (50ml)
150 mL NDC: 74765-011-02
236 mL NDC: 74765-011-03
500 mL NDC: 74765-011-04
* Please review the disclaimer below.
