Home NDC 71630-035 Deep Blue Mini
Product NDC 71630-035
11-digit product format 716300035
Labeler code 71630
Product ID 71630-035_51dd58a8-1fd6-9cd7-e063-6394a90a1f72
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form STICK
Route TOPICAL
Labeler doTERRA International, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-01
Substance MENTHOL, (+)-
Active strength 10 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 Deep Blue Mini
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, (+)- 10 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C6B1OE8P3W Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2475356 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71630-035-10 71630003510 1 TUBE in 1 BOX (71630-035-10) / 10 g in 1 TUBE 1 tube 2026-08-01 No No Current