NDC 68001-479

Pain Relieving

Pain Relieving

Pain Relieving is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Bluepoint Laboratories. The primary component is Menthol; Methyl Salicylate.

Product ID68001-479_dc73db77-ab4a-49fa-e053-2995a90ae501
NDC68001-479
Product TypeHuman Otc Drug
Proprietary NamePain Relieving
Generic NamePain Relieving
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2022-05-05
Marketing CategoryOTC MONOGRAPH NOT FINAL /
Application Numberpart348
Labeler NameBluePoint Laboratories
Substance NameMENTHOL; METHYL SALICYLATE
Active Ingredient Strength10 g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 68001-479-45

1 TUBE in 1 CARTON (68001-479-45) > 85.05 g in 1 TUBE
Marketing Start Date2022-05-05
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Pain Relieving" or generic name "Pain Relieving"

NDCBrand NameGeneric Name
11673-345Pain RelievingCamphor, Menthol, and Methyl Salicylate
24488-001Pain RelievingCamphor Menthol Methyl Salicylate
37205-824Pain RelievingMENTHOL
41250-559Pain RelievingFirst Aid Antiseptic and Pain Reliever
42217-207Pain RelievingCamphor, Menthol
43493-0002Pain RelievingCamphor, Menthol, Methyl Salicylate
61010-1560Pain Relievingmenthol, unspecified form
61010-4403Pain Relievingmenthol
63347-215Pain RelievingMENTHOL, CAMPHOR
68001-479Pain RelievingPain Relieving
68678-039Pain RelievingMenthol, Camphor, Capsaicin
72342-040Pain RelievingCAMPHOR (NATURAL)
72342-060Pain RelievingPhenol
69492-013BIOACTILPain Relieving

© 2022 FDA.report
This site is not affiliated with or endorsed by the FDA.