Active Ingredient
Ethyl Alcohol 75 % v/v
Medpride Antiseptic
FDA Label NDC 70814-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tongling Lin'ann Biological Technology Co., Ltd for the product Medpride Antiseptic (NDC 70814-001). 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, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if, 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
Antiseptic
Uses
■ for hand sanitizing to reduce bacteria on skin
Warnings
For external use only
■ flammable, keep away from fire or flame
Do Not Use
■ with electrocautery procedures ■ in the eyes■ if children less than 2 months of age■ on open skin wounds
When Using This Product
■ keep out of reach of eyes, ears and mouth
Stop Use And Ask A Doctor If
■if irritation and redness develop ■ if condition persists for more than 72 hours consult a doctor.
Keep Out Of Reach Of Children.
- If swallowed get medical help or contact Poison Control Center right away.
Directions
■discard after use■do not flush■close the lid properly after use
Other Information
■store at room temperature 15° - 30 ° C (59-86 F) ■avoid excessive heat
Inactive Ingredient
Aloe Vera Extract, Benzalkonium Chloride, Glycerin, Methyl Paraben, Phenoxyethanol, Propylene Glycol, water
* Please review the disclaimer below.
