Active Ingredient(S)
Alcohol 70% v/v;
Best-rx Moist Hand Wipes
FDA Label NDC 79904-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Best Equipment for the product Best-rx Moist Hand Wipes (NDC 79904-001). 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 ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Use
For hand sanitizing to decrease bacterial on the skin.
Warnings
For external use only. Flammable. Keep away from heat or flame
Do Not Use
- on infants less than 2 months of age
- on open skin wounds
Otc - When Using
When using this product avoid contact with eyes, flush with water immediately if contact is made or irritation occurs.
Otc - Stop Use
Discontinue use if irrtation or redness develops on skin.
Contact a doctor if condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children: Unless under adult supervision.
Directions
Tear open packet, wet hands thoroughly with towelette, allow hands to dry without wiping.
Discard after single use.
Inactive Ingredients
Inactive ingredients: Water
Package Label - Principal Display Panel
1 wipe in 1 pouch; NDC: 78183-001-01;
1pcs (1pcs)
* Please review the disclaimer below.
