Otc - Active Ingredient
Ethyl Alcohol
Novo Wipe Patch
FDA Label NDC 84449-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Benliju Bio-tech Co.,ltd for the product Novo Wipe (NDC 84449-009). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - 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
Otc - Purpose
Apply topically as needed to cleanse.
Indications & Usage
Apply topically as needed to cleanse.
Warnings
For external use only.
Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use with electrocautery procedures in the eyes. If contact occurs, flush eyes with water.
Otc - When Using
When using this product keep out of eyes.
Otc - Stop Use
Stop use if irritation and redness develop. If condition persists consult your health care practitioner.
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
Apply to skin as needed. Discard after single use.
Storage And Handling
Store at 59°F - 86°F (15°C - 30°C).
Inactive Ingredient
Purified Water
Package Label.Principal Display Panel
Package (Package)
* Please review the disclaimer below.
