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Drug Facts
Alcohol Wipes
FDA Label NDC 90059-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Qingdao Miuton Medical Co.,ltd. for the product Alcohol Wipes (NDC 90059-001). 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 other, active ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient(S)
Ethyl Alcohol 75%
Purpose
Antiseptic
Use
1.Hand Sanitizer to help decrease bacteria on the skin.
2.When water,soap & towel are not available.
3.Recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from fire or flame.
Do Not Use
Do not apply around eyes.
Do not use in ears & mouth.
Otc - When Using
When using this product avoid contact with eyes.In case of contact flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be supervised in use of this product.
Directions
Tear off the package and pull out the cotton piece, wipe and disinfect the skin.
Other Information
Store at 20C (88 to 77F) may discolor fabrices.
Inactive Ingredients
Water, spunlaced nonwovens.
* Please review the disclaimer below.
