FDA Label for Alcohol Pad
View Indications, Usage & Precautions
Alcohol Pad Product Label
The following document was submitted to the FDA by the labeler of this product Mckesson. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Isopropyl Alcohol 70% v/v
Purpose
Antiseptic
Use
For preparation of the skin prior to an injection
Warnings
For external use only. Flammable, keep away from fire or flame.
Do Not Use
- with electrocautery procedures
- in the eyes
Stop Use
If irritation and redness develop
Otc - Ask Doctor/Pharmacist
Otc - When Using
Ask A Doctor
If condition persists for more than 72 hours
Otc - Pregnancy Or Breast Feeding
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wipe injection site vigorously and discard
Other
Other Information
Store at room temperature 15° - 30° C (59° - 86° F)
Inactive Ingredient
Purified water
Otc - Questions
Package Information
Sunmark® COMPARE TO B-D® ACTIVE INGREDIENTS*NDC 49348-077-53Alcohol Prep PadsAntiseptic for preparation of the skin prior to injectionIsopropyl alcohol, 70%100 INDIVIDUALLY WRAPPED FOIL PACKETS1.25 X 1.25 IN (2.9 X 3.2 cm)Distributed by McKessonOne Post StreetSan Francisco, CA 94104Money Back Guarantee*This product is not namufactured or distributed by Beckton Dickson, owner of the registered trademark, B-D®.
* Please review the disclaimer below.
