Label: CAPSAICIN HEAT PATCHES BACK AND LARGE AREAS- capsaicin patch
- NDC Code(s): 41250-842-03
- 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 11, 2023
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- Official Label (Printer Friendly)
- For External Use Only
- Uses
- Purpose
- Active Ingredients
- Inactive Ingredients:
-
Directions for Use:
For Use on Adults and Childrens 12 Years of Age or Older
- Clean and dru affected area; ensure area is fully dry before application
- Remove patch from film
- Apply to treatement site
- Patch may be trimmerd to best fit treatment site; trim patch before removing film
- Wash hands after application
- Discard after signle use
Caution:
- Take care when using on elderly ot incapacited persons
- Do not use more than 8 hours
- Do not use the Capsaicin Heat Patch more than 3-4 times daily
- Do not exceed 7 days of continue use
- Keep Out of Reach of Children
- Storage and Care:
- Do Not Use:
- Use Only as Directed:
- Stop Use immediately and Seek Medical Attention if:
- QUESTIONS
- LABEL
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INGREDIENTS AND APPEARANCE
CAPSAICIN HEAT PATCHES BACK AND LARGE AREAS
capsaicin patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-842 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN 0.025 g in 100 g Inactive Ingredients Ingredient Name Strength HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) LIQUID PETROLEUM (UNII: 6ZAE7X688J) STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A) Product Characteristics Color Score Shape RECTANGLE Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-842-03 3 in 1 BOX 07/01/2018 1 9 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 06/01/2017 Labeler - Meijer Distribution Inc (006959555) Establishment Name Address ID/FEI Business Operations Foshan Aqua Gel Biotech Co.,Ltd. 529128763 manufacture(41250-842)