Active Ingredient
Ethyl Alcohol 66.5%
Antiseptic Gel
FDA Label NDC 72663-111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Welly Health Pcb for the product Antiseptic (NDC 72663-111). 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, purpose, uses, warnings, otc - keep out of reach of children, otc - do not use, otc - stop use, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For handwashing to decrease bacteria on skin without soap and water.
Warnings
External use only
Flammable, keep away from fire or flame.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Do Not Use
Do not use in eyes, if this happens, rinse thoroughly with water.
Otc - Stop Use
Stop use, ask a doctor if, irritation develops and persists for 72 hours. If ingested, get medical help or contact a Poison Control Center right away.
Directions
- Wet hands & wrists thoroughly with product and allow to dry without wiping
Inactive Ingredients
aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine
Welly Health PBC, Minn., MN 55402
1-833-BE-WELLY
Principal Display Panel - Welly Health Instant Hand Sanitizer Pouch Label
Welly™
Instant Hand
Sanitizer
0.9g/ 1/32 OZ
Principal Display Panel (Welly Health Instant Hand Sanitizer Pouch Label)
* Please review the disclaimer below.
