Home NDC 73096-745 CBDMEDIC Back and Neck Pain Relief
Product NDC 73096-745
11-digit product format 730960745
Labeler code 73096
Product ID 73096-745_2cc81b65-b0bc-1023-e063-6294a90a18de
Type HUMAN OTC DRUG
Nonproprietary name Camphor and Menthol
Dosage form OINTMENT
Route TOPICAL
Labeler ABACUS HEALTH PRODUCTS, INC.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-09-01
Substance CAMPHOR (NATURAL); MENTHOL
Active strength 100; 150 mg/g; mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base CBDMEDIC Back and Neck Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (NATURAL) 100 mg/g MENTHOL 150 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination N20HL7Q941 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73096-745-40 CBDMEDIC Back and Neck Pain Relief 40 g in 1 TUBE OINTMENT 40 5 73096-745-40 CBDMEDIC Back and Neck Pain Relief 1 in 1 CARTON OINTMENT 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73096-745 CBDMEDIC BACK AND NECK PAIN RELIEF (CAMPHOR AND MENTHOL) OINTMENT [ABACUS HEALTH PRODUCTS, INC.] 5 Current NDC, Legacy NDC, 2 package rows 20250130_f0ec8fc9-c401-5f23-e053-2995a90acb1c.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 8 of 156 · 3,115 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 73096-745-02 73096074502 1.7 g in 1 PACKET (73096-745-02) 1.7 g 2020-02-01 0000-00-00 No No Current 73096-745-04 73096074504 2 PACKET in 1 BLISTER PACK (73096-745-04) > 1.7 g in 1 PACKET 2 packet 2020-02-01 0000-00-00 No No Current 73096-745-07 73096074507 1 TUBE in 1 BLISTER PACK (73096-745-07) > 7 g in 1 TUBE 1 tube 2020-02-01 0000-00-00 No No Current 73096-745-40 73096074540 1 TUBE in 1 CARTON (73096-745-40) / 40 g in 1 TUBE 1 tube 2019-09-01 0000-00-00 No No Current