Active Ingredient(S)
Alcohol 75% by volume
Hand Sanitizing Alcohol Wipes
FDA Label NDC 80399-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jinhua Hongyuan Daily Chemicals Technology Co., Ltd. for the product Hand Sanitizing Alcohol Wipes (NDC 80399-001). 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, otc - keep out of reach of children, directions, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For hand sanitizing to decrease bacteria on the skin.
Apply topically to the skin to help prevent cross contamination.
Not recommended for repeated use.
Dries in seconds.
Warnings
.Flammable, Keep away from fire or flame. For external
use only.
. Do not use in or contact the eyes.
. Stop use and ask a doctor if too much skin irritation or sensitivity develops or increases.
Otc - Keep Out Of Reach Of Children
. Keep out of reach of children. If swallowed,
get medical help or contact a Poison control Center immediately
Directions
Open lid, gently pull back resealable label, remove and use wipe
Reseal back after use to avoid evaporation of alcohol.
Store at room temperature 15-30°C(59°-86°F).
Lot No. Manufacture date and Expiration date can be found on a package.
Inactive Ingredients
Water
Package Label - Principal Display Panel
1 (80399001)
* Please review the disclaimer below.
