Active Ingredients
Ethyl alcohol 15%. v/v
Benzalkonium Chloride 0.1%. v/v
Antiseptic Wipes
FDA Label NDC 80956-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by D&a Usa, Llc for the product Antiseptic Wipes (NDC 80956-001). 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 active ingredients, purpose, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Warnings
- For external use only.
Do Not Use
on children less than three years old and on skin wounds.
When Using This Product
Keep out of eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin.
Stop Use And Ask A Doctor If
irritation or rash appears and lasts.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Open lid, gently pull back resealable label, remove and use wipe as required.
- Reseal back after use to avoid evaporation of alcohol.
- Discard after single use Required dispose of used wipe in trash receptable.
- Do not flush.
Uses
- For hand washing to decrease bacteria on the skin.
- Apply topically to the skin to help prevent cross contamination.
Other Information
Store at room temperature, avoid sunlight irradiating.
Inactive Ingredients
Water, Cetylpyridinium chloride, Chlorphenesin, Biguanide, Propylene glycol
Package Label - Principal Display Panel
Pdp (79288 013 01)
* Please review the disclaimer below.
