Label: STING RELIEF- benzocaine,alcohol swab
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Contains inactivated NDC Code(s)
NDC Code(s): 35617-395-01 - Packager: NANTONG STRIP MEDICAL SUPPLY CO.,LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 May 26, 2010
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- Active Ingredient
- Use
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Directions
Apply to affected area not more than 3 to 4 times daily. For adults and children 2 years of age and older. Children under 2 years: consult a physician. DO NOT USE IN EYES, broken skin, deep puncture wounds, or if unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately
- Cautions
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STING RELIEF
benzocaine,alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:35617-395 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5) Benzocaine 0.06 mL Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 0.6 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:35617-395-01 1 in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 05/24/2010 Labeler - NANTONG STRIP MEDICAL SUPPLY CO.,LTD. (546585519) Establishment Name Address ID/FEI Business Operations NANTONG STRIP MEDICAL SUPPLY CO.,LTD. 546585519 manufacture