Aq Pure Instant Hand Sanitizer
FDA Label NDC 79333-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Day Great Llc for the product Aq Pure Instant Hand Sanitizer (NDC 79333-001). 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 drug facts, active ingredients, purpose, uses:, directions:, warnings:, do not use, when using this product,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Alcohol 80%
Purpose
Antiseptic
Uses:
- wet hands bacteria on the skin that could disease
- recommended for repeated uses
Directions:
- wet hands thoroughly with product and allow to dry without wiping
- not recommende for infants
Warnings:
- For external use only
- Flammable
- Keep away from heat and flame
- Do not store above 40 degrees Celcius (15 degrees Farenheit)
Do Not Use
- in mouth, ears or eyes
When Using This Product,
- avoid contact with eyes
- In case of contact, flush eyes with water
Stop Use And Seek A Doctor
- if redness or irritation develops and persist for more than 72 hours
- Children must be supervise in use of this product
- Pump as needed into your palms and thoroughly spread on both hands
- Rub in to skin until dry
Keep Out Of Reach Of Children
- children must be supervised in the use of this product
Other Information:
- may discolor some fabrics
- harmful to wood finishes and plastics
Inactive Ingredients:
- water
- triethanolamine
- acrylates/c 10-30 alkyl crosspolymer
- glycerin
Package Labeling:290Ml
Bottle (Bottle)
Package Labeling:480Ml
Bottle2 (Bottle2)
* Please review the disclaimer below.
