Active Ingredient
Benzalkonium chloride 0.13% (w/w)
Sanidry Wipes
FDA Label NDC 77251-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Quimica Rosmar S.a. De C.v. for the product Sanidry Wipes (NDC 77251-002). 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, purpose, uses, warnings, otc - when using, otc - stop use, otc - 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
Uses
- For hand sanitizing to decrease bacteria on the skin when water and soap are not available
- Recommended for repeated use.
Warnings
For external use only. Flammable: keep away from fire or flame.
Otc - When Using
When using this product do not use in near eyes. If contact occurs, flush thoroughly with water.
Otc - Stop Use
Stop use and contact a doctor if irritation or redness persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Remove wipe
- Wet hand thoroughly with wipe and allow hands to dry without wiping.
Inactive Ingredients
water, ethyl alcohol, glycerin, tetrasodium EDTA
Other Information
- Store at temperature below 110 F (43°C)
- May discolor certain fabrics or surfaces
Package Label.Principal Display Panel
300 Wipes - NDC 77251-002-01
Label-77251-002-01 (Label 77251 002 01)
1200 Wipes - NDC 77251-002-02
Label-77251-002-02 (Label 77251 002 02)
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