Active Ingredient(S)
Alcohol 75%
Alcohol Wipes
FDA Label NDC 78781-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shandong Oushile Biotechnology Co.ltd for the product Alcohol Wipes (NDC 78781-006). 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
Antisepticnactive
Use
Sterilization for hands and skin
Warnings
For external use only.
These wipes do not replace wipes used for medical procedures.
These wipes are meant for general cleansing.
Keep in a dry place away from fire.
Do Not Use
Do not use in or contact the eyes.
Otc - When Using
These wipes are meant for general cleansing.
Keep in a dry place away from fire.
Otc - Stop Use
Discontinue use if irritation and redness develop. If the condition persists for more than 72 hours, consult a physician.
Otc - Keep Out Of Reach Of Children
Keep this out of reach of children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Please close the lid after dispensing to maintain purity, Alcohol by nature evaporates quickly.
Other Information
Store below 95°F(35°C)
Inactive Ingredients
Aqua (Purified& De-lonied Water), Glycerin, Cetylpyridinium Chloride, Aloe Barbadensis leaf extract
Package Label - Principal Display Panel
P (Packaging)
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