Label: KROGER PAIN RELIEF LIDOCAINE PATCH- lidocaine patch
- NDC Code(s): 30142-583-06
- Packager: Kroger Company
- 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 April 3, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not Use
-
When using this product
1. Use only as directed
2. Read and follow all directions and warnings on this carton
3. Do not allow contact with the eyes
4. Do not use at the same time as other topical analgesics
5. Do not bandage tightly or apply local heat (such as heating pads) to the area of use
6. Do not microwave
7. Dispose of used patch in manner that always keeps product away from children or pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.
- Stop use and consult a doctor
- If pregnant or breastfeeding
- Keep out of reach of children and pets
- Directions
- Other Information
- Inactive Ingredients
- Kroger Pain Relief 4% Lidocaine Patch
-
INGREDIENTS AND APPEARANCE
KROGER PAIN RELIEF LIDOCAINE PATCH
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-583 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 100 g Inactive Ingredients Ingredient Name Strength KAOLIN (UNII: 24H4NWX5CO) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F) PETROLATUM (UNII: 4T6H12BN9U) GLYCERIN (UNII: PDC6A3C0OX) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) TARTARIC ACID (UNII: W4888I119H) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) PHENOXYETHANOL (UNII: HIE492ZZ3T) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) WATER (UNII: 059QF0KO0R) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-583-06 6 in 1 CARTON 04/01/2023 1 1 g in 1 PATCH; 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 04/01/2023 Labeler - Kroger Company (006999528) Establishment Name Address ID/FEI Business Operations Foshan Aqua Gel Biotech LLC 529128763 manufacture(30142-583)