Snugell Spray
FDA Label NDC 80671-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Quanzhou Aiwina Hygiene Products Co.,ltd for the product Snugell (NDC 80671-005). 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 ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.13% (w/w)
Purpose
Antiseptic
Uses
Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only.
Do Not Use
• On children less than 2 months of age
• Near eyes or on open skin wounds
When using this product avoid contacting with eyes. In case of eye contact, rinse eyes with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away at 800-222-1222.
Directions
• Sprays over the desired skin surface area and rub thoroughly. No rinse is required.
• Children under 6 years of age should be supervised when using this product.
Other Information
• Avoid freezing and store below 110F (43C).
• Dispose of the empty can in a recycling bin.
Inactive Ingredients
Aloe barbadensis leaf extract, butylene glycol, chamomilla recutita (matricaria) extract, grape seed extract, purified water.
Questions Or Comments?
Call 1-844-451-6555
Packaging
Image (80671 005 33 4)
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