Otc - Active Ingredient
Ethyl Alcohol - 76%
Antiseptic Wipes Swab
FDA Label NDC 57362-469
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Westwood Laboratories for the product Antiseptic Wipes (NDC 57362-469). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Indications & Usage
- To decrease bacteria on skin.
- Recommended for repeated use.
Warnings
- For external use only
- Flammable. Keep away from flames or fires.
Otc - When Using
- Do not used in or near eyes.
- In case of contact, wash eyes thoroughly with water.
- Avoid contact with broken skin.
- Do not inhale or ingest.
Otc - Stop Use
- Irritiation or redness develops.
- Condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or call a Poison Control Center right away.
Dosage & Administration
- Wet hands thoroughly with product and let dry without wiping.
- For children under 6, use only with adult supervision.
- Not recommended for use on infants.
Storage And Handling
Store 20-25*C (66-77*F)
Inactive Ingredient
Benzethonium Chloride, Dimethicone, Farnesol, Panthenol, PEG-12, Polyaminopropyl Biguanide, Water.
Package Label.Principal Display Panel
Single Wipe Labeling
NDC: 57362-469-18
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