Label: HOT AND COLD LIDOCAINE WITH MENTHOL PATCH PAIN RELIEF- lidocaine and menthol patch
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Contains inactivated NDC Code(s)
NDC Code(s): 76168-099-11 - Packager: Velocity Pharma LLC
- 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 3, 2017
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
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Warnings
For external use only.
Do not use if you are allergic or sensitive to lidocaine or menthol. Do not use if pouch is damaged or opened.
When using this product
- use only as directed
- avoid contact with eyes or mucous membranes
- do not apply to open wounds or sensitive skin
- do not bandage tightly or use a heating pad
- Directions
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Inactive Ingredients
aluminium hydroxide gel, bentonite, borax, carbomer, carboxymethylcellulose sodium,
colloidal silicon dioxide, dihydroxyaluminumaminoacetate, disodiumedetate, gelatin, glycerin, oleic acid, polysorbate 80, polyvinyl Alcohol, potassium Sorbate, povidone, propylene glycol, sodiummetabisulphite, tartaric acid, trolamine, urea, water - PRINCIPAL DISPLAY PANEL - 3 Topical Patch Carton
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INGREDIENTS AND APPEARANCE
HOT AND COLD LIDOCAINE WITH MENTHOL PATCH PAIN RELIEF
lidocaine and menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76168-099 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10 mg Inactive Ingredients Ingredient Name Strength ALGELDRATE (UNII: 03J11K103C) BENTONITE (UNII: A3N5ZCN45C) SODIUM BORATE (UNII: 91MBZ8H3QO) CARBOMER 940 (UNII: 4Q93RCW27E) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) OLEIC ACID (UNII: 2UMI9U37CP) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) POVIDONE (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TARTARIC ACID (UNII: W4888I119H) UREA (UNII: 8W8T17847W) WATER (UNII: 059QF0KO0R) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) TROLAMINE (UNII: 9O3K93S3TK) SODIUM METABISULFITE (UNII: 4VON5FNS3C) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76168-099-11 5 in 1 CARTON 03/03/2017 1 1 in 1 POUCH; 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 03/03/2017 Labeler - Velocity Pharma LLC (962198409) Registrant - Velocity Pharma LLC (962198409) Establishment Name Address ID/FEI Business Operations DR SABHARWALS WOUND CARE 862184668 manufacture(76168-099)