Active Ingredients
Isopropyl Alcohol USP, 70% v/v
Alcohol Prep
FDA Label NDC 68113-520
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Caribbean Medical Brokers, Inc for the product Alcohol Prep (NDC 68113-520). 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 ingredients, purpose, use, warnings:, otc - keep out of reach of children, caution:, otc - do not use, directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For preparation of the skin prior to injection; to decrease germs in minor cuts and scrapes.
Warnings:
For external use only. Flammable; keep away from fire and flame.
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.
Caution:
Do not apply to irritated skin.
Otc - Do Not Use
Do not use in the eyes, or on mucous membranes.
In case of deep or puncture wounds, consult a doctor.
Directions:
Wipe injection site vigorously.
Other Information:
Store at room temperature.
Inactive Ingredients:
Water
Principal Display Panel
50 Individual Pads
SMS Specialty Medical Supplies
Alcohol Prep Pads
Extra Thick Soft Pad!
Antiseptic for preparation of skin prior to injection
For Individual, Professional, and Hospital Use
Saturated with 70% v/v Isopropyl Alcohol for external use only
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