Inactive Ingredient
Inactive Ingredients
carbomer 940, glycerin,
propylene glycol, red 33,
tocopheryl acetate,
triethonamoline, water
Alcohol
FDA Label NDC 43473-805
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nantong Health & Beyond Hygienic Products Inc. for the product Alcohol (NDC 43473-805). 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 inactive ingredient, otc - active ingredient, otc - purpose, warnings, otc - keep out of reach of children, dosage & administration, indications & usage, otc - do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol, 65 % v/v
Otc - Purpose
Purpose Antimicrobial
Warnings
Warnings
For external use only
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.
Dosage & Administration
Directions. Put a dime sized
drop onto hands and rub
briskly until dry.
Indications & Usage
Uses. hand sanitizer to help
reduce bacteria on skin
Otc - Do Not Use
Do not use in or near the eyes.
In case of contact, rinse eyes
thoroughly with water.
Other Safety Information
Flammable. Keep away from
fire or flame
Otc - Stop Use
Stop use and ask a doctor
if irritation, excessive redness
or rash develops
Storage And Handling
Other information
Store below 110 F ( 43 C)
Package Label.Principal Display Panel
Copy Of Label (Nantong Vanilla)
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