Active Ingredients
Benzalkonium Chloride 0.10%
1200 Wet Wipes
FDA Label NDC 77081-001
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 D Office Products, Inc. for the product 1200 Wet Wipes (NDC 77081-001). 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, use, warnings, otc - keep out of reach of children, additional information:, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Sanitizing
Use
hand sanitizer to decrease bacteria on the skin.
Warnings
For external use only.
Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.
Do not use if you are allergic to any of the ingredients.
Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children unless under adult supervision.
If swallowed, get medical help
Additional Information:
• Store below 110°F (43°C).
• May discolor certain fabrics or surfaces.
Inactive Ingredients
Sodium Carboxymethyl Lauryl Glucoside, Sodium PCA, Cocamide DEA, Citric Acid, Parfum / Fragrance, Ethyl glycerin, Vitamin E, Water, Aloe Essence Extract, Phenoxyethanol
Packaging
Image (7708100112)
* Please review the disclaimer below.
