Active Ingredient(S)
Hexamine:0.23%-0.27%
Benzalkonium bromide:0.12%-0.14%
Sanitizer
FDA Label NDC 93068-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kangsheng Medical Technology (wenzhou) Co. , Ltd for the product Sanitizer (NDC 93068-003). 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
Use
To decrease bacteria on the skin that could cause disease
recommended for repeat use
Use without water
Warnings
For external use only.
Keep out of reach of children, in case of accidental ingestion,seek professional assistance.
Discontinue if skin becomes irritated and ask a doctor
Do not use it together with peroxide and detergent
Keep in a cool and dry place
Do Not Use
it together with peroxide and detergent
Otc - When Using
.
Otc - Stop Use
discontinue if skin becomes irritated and ask a doctor
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.in case if accidental ingestion,seek professional assistance
Directions
Wet hands throughly with product and rub until dry without wiping
For children under 6 years old,use only under adult supervision
Inactive Ingredients
water
Package Label - Principal Display Panel
Package Label (Ce3612b8b3c8e8061c1d24d8afcee81)
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