Label: ALCOHOL PREP PADS WITH PAIN RELIEF- alcohol and benzocaine swab
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Contains inactivated NDC Code(s)
NDC Code(s): 49614-221-44 - Packager: Medicine Shoppe International Inc
- 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 March 15, 2010
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
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DIRECTIONS
Prior to Injection - Adults and children 2 years of age or older:
Apply to the skin just prior to injection. Benzocaine takes a minute to act. for best results, wait briefly and then make injection.
Insect bites, skin irritations, minor burns, sunburn -
Adults and children 2 years of age or older:
Apply to the affected site not more than 3 to 4 times daily.
Children under 2 years of age: Ask a doctor.
- SPL UNCLASSIFIED SECTION
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS
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CARTON INFORMATION
The Medicine Shoppe®
NEW!
WITH PAIN RELIEF
NDC 49614-221-44
Alcohol Swabs
with Benzocaine for PAIN RELIEF80 Individually wrapped swabs
Distributed by Medicine Shoppe International, Inc.
St. Louis, MO 63162
www.medicineshoppe.com
A Cardinal Health Company;
CIN 3985363
MEDICINE SHOPPE® GUARANTEE
IF YOU ARE NOT FULLY SATISFIED
WITH THIS PRODUCT, SIMPLY RETURN
THE UNUSED PORTION FOR REPLACEMENT
OR FULL REFUND OF PURCHASE PRICE.
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INGREDIENTS AND APPEARANCE
ALCOHOL PREP PADS WITH PAIN RELIEF
alcohol and benzocaine swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49614-221 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength benzocaine (UNII: U3RSY48JW5) (benzocaine - UNII:U3RSY48JW5) benzocaine 0.06 mL isopropyl alcohol (UNII: ND2M416302) (isopropyl alcohol - UNII:ND2M416302) isopropyl alcohol 0.70 mL Inactive Ingredients Ingredient Name Strength propylene glycol (UNII: 6DC9Q167V3) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49614-221-44 80 in 1 CARTON 1 1 in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 06/28/2007 Labeler - Medicine Shoppe International Inc (071997654)