Active Ingredient(S)
Ethyl Alcohol 75% v/v. Purpose: Antiseptic
Wet Wipes
FDA Label NDC 78736-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Huangshan Nanguozhichun Tourists Products Co., Ltd. for the product Wet Wipes (NDC 78736-001). 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 - 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
Use
Decreases bacteria on skin. Recommended for repeated use
Warnings
For external use only.Do not use over large areas of the body if you are allergic to any of the ingredients when using this product,avoid contact with eyes and face.If contact occurs,flush thoroughly with water.Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
For adults and children of 2 years and over.children under 2 years ask a doctor before use allow to dry without wiping.
Inactive Ingredients
Purified water
Package Label - Principal Display Panel
1 pc in bag NDC: 78736-001-01
Label-1 Pc (Label 1wipe)
10 pcs in bag NDC: 78736-001-02
Label-10pcs (Label 10wipes)
50 pcs in bag NDC: 78736-001-03
Label-50pcs (Label 50wipes)
* Please review the disclaimer below.
