NDC 47682-235

Medi-First Pain Relief

Analgesic- Menthol

Medi-First Pain Relief is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Unifirst First Aid Corporation. The primary component is Menthol.

Product ID47682-235_8154a8f2-290d-06e3-e053-2a91aa0a5f41
NDC47682-235
Product TypeHuman Otc Drug
Proprietary NameMedi-First Pain Relief
Generic NameAnalgesic- Menthol
Dosage FormSpray
Route of AdministrationTOPICAL
Marketing Start Date2019-04-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NameUnifirst First Aid Corporation
Substance NameMENTHOL
Active Ingredient Strength70 mg/L
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 47682-235-02

.059 L in 1 BOTTLE, SPRAY (47682-235-02)
Marketing Start Date2019-04-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 47682-235-02 [47682023502]

Medi-First Pain Relief SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-04-01

Drug Details

Active Ingredients

IngredientStrength
MENTHOL70 mg/L

OpenFDA Data

SPL SET ID:8154a8f2-290c-06e3-e053-2a91aa0a5f41
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1086713
  • UPC Code
  • 0347682231026

  • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.