Label: STING RELIEF- alcohol, lidocaine hydrochloride cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 0924-5200-01, 0924-5200-02, 0924-5200-03 - Packager: Acme United Corporation
- 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 22, 2016
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INGREDIENTS AND APPEARANCE
STING RELIEF
alcohol, lidocaine hydrochloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0924-5200 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M) alcohol 0.50 mL in 1 mL lidocaine hydrochloride (UNII: V13007Z41A) (lidocaine - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength benzalkonium chloride (UNII: F5UM2KM3W7) menthol (UNII: L7T10EIP3A) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0924-5200-02 10 in 1 BOX 03/06/2012 1 NDC:0924-5200-01 0.9 mL in 1 PACKET; Type 0: Not a Combination Product 2 NDC:0924-5200-03 50 in 1 BOX 03/06/2012 2 NDC:0924-5200-01 0.9 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/06/2012 Labeler - Acme United Corporation (001180207) Registrant - Safetec of America, Inc. (874965262) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc. 874965262 MANUFACTURE(0924-5200)