Active Ingredient(S)
benzalkonium chloride 0.13%
Sanitizing Wipes
FDA Label NDC 80991-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Fanjia Medical Equipment Co., Ltd. for the product Sanitizing Wipes (NDC 80991-003). 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, inactive ingredients, uses, 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
Purpose
Antimicrobial
Inactive Ingredients
Aqua,Isopropyl alcohol, Propylene glycol, Tocopherol acetate, polysorbote 20, phenoxyethanol, Perfume
Uses
Suitable for skin cleaning and sterilization
Warnings
For external use only.
Flammable,keep away from fire or flame
Do Not Use
- on open skin wounds
Otc - When Using
When using this product, avoid contact with eyes.In case of contact with eyes, rinse with water to remove.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develop.
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
Directions
- Wet hands thoroughly with product and allow to dry without wiping
Other Information
- Do not store above 110F
- May discolor some fabrics
Package Label - Principal Display Panel
160PCS NDC 80991-003-01
160PCS NDC 80991-003-02
160PCS NDC 80991-003-03
160PCS NDC 80991-003-04
003-04 (80991 003 04)
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