Label: ALCOHOL PAD- isopropyl alcohol swab
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Contains inactivated NDC Code(s)
NDC Code(s): 49348-077-53 - Packager: McKesson
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 4, 2010
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- ACTIVE INGREDIENT
- PURPOSE
- USE
- WARNINGS
- DIRECTIONS
- SPL UNCLASSIFIED SECTION
- OTHER INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
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PACKAGE INFORMATION
Sunmark®
COMPARE TO B-D® ACTIVE INGREDIENTS*
NDC 49348-077-53
Alcohol Prep Pads
Antiseptic for preparation of the skin prior to injection
Isopropyl alcohol, 70%
100 INDIVIDUALLY WRAPPED FOIL PACKETS
1.25 X 1.25 IN (2.9 X 3.2 cm)
Distributed by McKesson
One Post Street
San Francisco, CA 94104
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*This product is not namufactured or distributed by Beckton Dickson, owner of the registered trademark, B-D®.
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INGREDIENTS AND APPEARANCE
ALCOHOL PAD
isopropyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49348-077 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Isopropyl alcohol (UNII: ND2M416302) (Isopropyl alcohol - UNII:ND2M416302) Isopropyl alcohol 0.70 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49348-077-53 100 in 1 BOX 1 1 in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/19/2003 Labeler - McKesson (177667227)