NDC 67510-0058

Oral Pain Relief

Oral Pain Reliever

Oral Pain Relief is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Kareway Product, Inc.. The primary component is Benzocaine.

Product ID67510-0058_615afe0d-b55d-8efc-e053-2991aa0ab306
NDC67510-0058
Product TypeHuman Otc Drug
Proprietary NameOral Pain Relief
Generic NameOral Pain Reliever
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2011-07-17
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart356
Labeler NameKareway Product, Inc.
Substance NameBENZOCAINE
Active Ingredient Strength200 mg/g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 67510-0058-4

1 TUBE in 1 CARTON (67510-0058-4) > 11.9 g in 1 TUBE
Marketing Start Date2011-07-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67510-0058-4 [67510005804]

Oral Pain Relief GEL
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-07-17
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BENZOCAINE200 mg/g

OpenFDA Data

SPL SET ID:b5d833d9-e367-4927-8e4f-790ad41d2502
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 238910
  • NDC Crossover Matching brand name "Oral Pain Relief" or generic name "Oral Pain Reliever"

    NDCBrand NameGeneric Name
    47046-156Oral Pain ReliefBenzocaine and Benzalkonium Chloride
    52000-060Oral Pain ReliefBenzocaine and Benzalkonium Chloride
    53943-996Oral Pain ReliefOral Pain Reliever
    57896-139Oral Pain ReliefBENZOCAINE
    67510-0058Oral Pain ReliefOral Pain Reliever
    41250-701Oral AnalgesicOral Pain Reliever

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