Label: KROGER LIDOCAINE PAIN RELIEVING- lidocaine hcl liquid
- NDC Code(s): 41226-740-01
- Packager: Kroger Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
On large areas of the body or on cut, irritated or swollen skin
■ on puncture wounds■for more than one week without consulting a doctor
When using this product
■use only as directed. Read and follow all directions and warnings on this carton
■do not allow contact with the eyes and mucous membranes
■ do not bandage or apply local heat (such as heating pads) or a medicated patch to area of use
■do not use at the same time as other topical analgesics
- Directions
- Other information
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Inactive Ingredients
acrylates/C10-30 alkyl acrylate crosspolymer (60000 MPA.S), aloe barbadensis leaf juice, am nomethylpropanol, ceteth-10 phosphate, cetostearyl alcohol, cyclomethicone 5, dicetyl phosphate, dimethicone 350, dimethicone/vinyl dimethicone crosspolymer (soft particle),
disodium EDTA, ethylhexylglycerin, glyceryl 1 stearate, hydroxyethyl acrylate/sodium acryloyld methyl taurate copolymer (100000 MPA.S at 1.5%), sohexadecane, phenoxyethanol, SD alcohol, steareth-21, water
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INGREDIENTS AND APPEARANCE
KROGER LIDOCAINE PAIN RELIEVING
lidocaine hcl liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41226-740 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 1 mL Inactive Ingredients Ingredient Name Strength DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) DIMETHICONE 350 (UNII: 2Y53S6ATLU) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALCOHOL (UNII: 3K9958V90M) ALOE VERA LEAF (UNII: ZY81Z83H0X) STEARETH-21 (UNII: 53J3F32P58) ISOHEXADECANE (UNII: 918X1OUF1E) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41226-740-01 1 in 1 CARTON 04/01/2024 1 73 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/01/2024 Labeler - Kroger Company (006999528) Establishment Name Address ID/FEI Business Operations Nantong Health & Beyond Hygienic Products Inc. 421280161 manufacture(41226-740)