Home NDC 71805-855 TerraFreeze Pain Relief
Product NDC 71805-855
11-digit product format 718050855
Labeler code 71805
Product ID 71805-855_09dc09a4-8c6f-1ab6-e063-6394a90a8b1d
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL,METHYL SALICYLATE,HISTAMINE DIHYDROCHLORIDE
Dosage form CREAM
Route TOPICAL
Labeler Beyond Derma, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-10-12
Substance MENTHOL; METHYL SALICYLATE; HISTAMINE DIHYDROCHLORIDE
Active strength 100; 100; .5 mg/g; mg/g; mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 TerraFreeze Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 100 mg/g METHYL SALICYLATE 100 mg/g HISTAMINE DIHYDROCHLORIDE .5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup LAV5U5022Y Internal UNII lookup 3POA0Q644U Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1947261 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71805-855-00 TerraFreeze Pain Relief 57 g in 1 PACKAGE CREAM 57 2 71805-855-00 TerraFreeze Pain Relief 1 in 1 BOX CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71805-855 TERRAFREEZE PAIN RELIEF (MENTHOL,METHYL SALICYLATE,HISTAMINE DIHYDROCHLORIDE) CREAM [BEYOND DERMA, LLC] 2 Current NDC, Legacy NDC, 2 package rows 20231112_81dc70b3-7e93-4f9a-ae3a-b50bbfd1a677.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71805-855-00 71805085500 1 PACKAGE in 1 BOX (71805-855-00) / 57 g in 1 PACKAGE 1 package 2017-10-12 0000-00-00 No No Current