Label: LIDOCAINE HYDROCHLORIDE gel
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Contains inactivated NDC Code(s)
NDC Code(s): 0924-5000-00, 0924-5000-01, 0924-5000-02 - Packager: Acme United Corporation
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 7, 2016
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- Active ingredients
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- Inactive ingredients
- Principal Display Panel - Pouch Label
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INGREDIENTS AND APPEARANCE
LIDOCAINE HYDROCHLORIDE
lidocaine hydrochloride gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0924-5000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lidocaine Hydrochloride (UNII: V13007Z41A) (Lidocaine - UNII:98PI200987) Lidocaine Hydrochloride Anhydrous 20 mg in 1 g Inactive Ingredients Ingredient Name Strength aloe vera leaf (UNII: ZY81Z83H0X) propylene glycol (UNII: 6DC9Q167V3) diazolidinyl urea (UNII: H5RIZ3MPW4) water (UNII: 059QF0KO0R) menthol (UNII: L7T10EIP3A) .alpha.-tocopherol acetate (UNII: 9E8X80D2L0) trolamine (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0924-5000-01 6 in 1 BOX 02/14/2013 1 NDC:0924-5000-00 3.5 g in 1 PACKET; Type 0: Not a Combination Product 2 NDC:0924-5000-02 25 in 1 BOX 02/14/2013 2 NDC:0924-5000-00 3.5 g 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 part348 02/14/2013 Labeler - Acme United Corporation (001180207) Registrant - Safetec of America, Inc. (874965262) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc. 874965262 MANUFACTURE(0924-5000)