Label: KO PINK PAIN RELIEF CREAM- lidocaine hcl and phenolate sodium cream
- NDC Code(s): 70317-005-01
- Packager: Remeverse
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 16, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
-
Inactive Ingredients
Water, Caprylic/Capric Triglyceride, Glycerin, Calendula Officinalis Flower Extract, Glyceryl Stearate, Sodium Hyaluronate, Butylene Glycol, Cetyl Alcohol, Sodium Hydroxide, Isonononyl Isononanoate, Stearic Acid, Thioctic Acid (Alpha Lipoic Acid) powder, Carbomer, Cetearyl 2-Ethylhexanoate, Dimethylsulfone (MSM), Polysorbate 80, Hydroxypropyl Methylcellulose, N-Acetyl Glucosamine, SYN-TC, Polysorbate 20, Palmitoyl Oligopeptide, Palmitoyl Tetrapeptide-7, Tocopheryl Acetate (Vitamin E), Phytonadione (Vitamin K), Benfotiamine, Curcumin, Ceramide 3, 3-glyceryl Ascorbate (Vitamin C), Pyridoxine Hydrochloride, Cyanocobalamin, Cyclodextrin, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol
- Directions
- Use
- Stop Use
- Warning - Keep out of reach of children
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Warnings
For external use only
Do not use:
- In large quantities
- Over raw surfaces or blistered areas
- if you are allergic to ingredients in this product
- on puncture wounds
- Over large areas of the body
When using this product:
- use only as directed
- do not bandage tightly or apply local heat (such as heating pads) to the area of use
- avoid contact with eyes, lips and mouth
- do not apply to wounds, damaged, broken or irritated skin
- Storage
- Purpose
- Pregnant or Breastfeeding
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KO PINK PAIN RELIEF CREAM
lidocaine hcl and phenolate sodium creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70317-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 0.04 g in 1 mL PHENOLATE SODIUM (UNII: 4NC0T56V35) (PHENOL - UNII:339NCG44TV) PHENOLATE SODIUM 0.005 g in 1 mL Inactive Ingredients Ingredient Name Strength CYCLODEXTRINS (UNII: 7E6SK9QDT8) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CETYL ALCOHOL (UNII: 936JST6JCN) CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCERIN (UNII: PDC6A3C0OX) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) N-ACETYLGLUCOSAMINE (UNII: V956696549) CERAMIDE 3 (UNII: 4370DF050B) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) SODIUM HYDROXIDE (UNII: 55X04QC32I) STEARIC ACID (UNII: 4ELV7Z65AP) THIOCTIC ACID (UNII: 73Y7P0K73Y) POLYSORBATE 80 (UNII: 6OZP39ZG8H) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) CYANOCOBALAMIN (UNII: P6YC3EG204) PHENOXYETHANOL (UNII: HIE492ZZ3T) PHYTONADIONE (UNII: A034SE7857) TETRADECYL AMINOBUTYROYLVALYLAMINOBUTYRIC UREA TRIFLUOROACETATE (UNII: 0UBP26S1LG) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) POLYSORBATE 20 (UNII: 7T1F30V5YH) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) BENFOTIAMINE (UNII: Y92OUS2H9B) PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) WATER (UNII: 059QF0KO0R) CURCUMIN (UNII: IT942ZTH98) 3-GLYCERYL ASCORBATE (UNII: 3R1Q5X5GGO) HEXYLENE GLYCOL (UNII: KEH0A3F75J) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO) PALMITOYLLYSYLVALYLDIAMINOBUTYROYLTHREONINE (UNII: 1615WE9073) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70317-005-01 118 mL in 1 JAR; Type 0: Not a Combination Product 09/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 09/01/2023 Labeler - Remeverse (050186540) Registrant - Lexia LLC (015552120) Establishment Name Address ID/FEI Business Operations Lexia LLC 015552120 manufacture(70317-005)