Label: MEIJER ODOR FREE ANALGESIC PAIN RELIEVING TOPICAL ANALGESIC- lidocaine hydrochloride liquid
- NDC Code(s): 41250-351-01
- Packager: Meijer Distribution, 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 January 19, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
When using this product
- ◆
- avoid contact with eyes
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- do not apply to wounds or damaged skin
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- do not bandage tightly
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- do not use with heating pads or other heating devices
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- as with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product
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- do not use in large quantities, particularly over raw surfaces or blistered areas
- Directions
- Other information
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Inactive ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Alcohol denat., Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Caprylyl Methicone, Cetearyl Alcohol, Ceteth-20 Phosphate, Dicetyl Phosphate, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Glyceryl Stearate, Isodexadecane, Phenoxyethanol, Polysorbate 60, Steareth-21, Water.
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 74 mL Cylinder Carton
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INGREDIENTS AND APPEARANCE
MEIJER ODOR FREE ANALGESIC PAIN RELIEVING TOPICAL ANALGESIC
lidocaine hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-351 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) Alcohol (UNII: 3K9958V90M) Aloe Vera Leaf (UNII: ZY81Z83H0X) Aminomethylpropanol (UNII: LU49E6626Q) Caprylyl Trisiloxane (UNII: Q95M2P1KJL) Cetostearyl Alcohol (UNII: 2DMT128M1S) Ceteth-20 Phosphate (UNII: 921FTA1500) Dihexadecyl Phosphate (UNII: 2V6E5WN99N) Dimethicone (UNII: 92RU3N3Y1O) Edetate Disodium (UNII: 7FLD91C86K) Ethylhexylglycerin (UNII: 147D247K3P) Glyceryl Monostearate (UNII: 230OU9XXE4) Isohexadecane (UNII: 918X1OUF1E) Phenoxyethanol (UNII: HIE492ZZ3T) Polysorbate 60 (UNII: CAL22UVI4M) Steareth-21 (UNII: 53J3F32P58) Water (UNII: 059QF0KO0R) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-351-01 1 in 1 CARTON 02/27/2019 1 74 mL in 1 CYLINDER; 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 02/27/2019 Labeler - Meijer Distribution, INC (006959555) Registrant - Garcoa, Inc. (036464697) Establishment Name Address ID/FEI Business Operations Sigan Industries INC. 255106239 MANUFACTURE(41250-351)