Home NDC 71856-176 Arctic Blast Pain Releiving
Product NDC 71856-176
11-digit product format 718560176
Labeler code 71856
Product ID 71856-176_2ffc226d-1051-58a4-e063-6294a90a349b
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, CAMPHOR (SYNTHETIC)
Dosage form LIQUID
Route TOPICAL
Labeler Nutriomo Labs Pte, Ltd
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-05-01
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Active strength 100; 30 mg/mL; mg/mL
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 Arctic Blast Pain Releiving
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 100 mg/mL CAMPHOR (SYNTHETIC) 30 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 5TJD82A1ET Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1987413 Internal RxNorm 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 71856-176-01 Arctic Blast Pain Releiving 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71856-176 ARCTIC BLAST PAIN RELEIVING (MENTHOL, CAMPHOR (SYNTHETIC)) LIQUID [NUTRIOMO LABS PTE, LTD] 3 Current NDC, Legacy NDC, 1 package rows 20250311_d5e7d26d-4f63-4b7b-a173-fe3a794c8459.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 48 of 153 · 3,057 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 71856-176-01 71856017601 30 mL in 1 BOTTLE, DROPPER (71856-176-01) 30 ml 2018-05-01 0000-00-00 No No Current