Home NDC 75638-009 Doctor Hoys Arnica Boost Recovery
Product NDC 75638-009
11-digit product format 756380009
Labeler code 75638
Product ID 75638-009_4769bbc4-c164-6de3-e063-6294a90a225f
Type HUMAN OTC DRUG
Nonproprietary name ARNICA MONTANA
Dosage form GEL
Route TOPICAL
Labeler Dynamic Blending Specialists, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-03-01
Marketing end 2028-04-17
Substance ARNICA MONTANA
Active strength 50 mg/mL
NDC exclude flag No
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 · 12 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 Doctor Hoys Arnica Boost Recovery Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O80TY208ZW Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 75638-009-00 Doctor Hoys Arnica Boost Recovery 89 mL in 1 TUBE GEL 89 3 75638-009-01 Doctor Hoys Arnica Boost Recovery 177 mL in 1 TUBE GEL 177 3 75638-009-02 Doctor Hoys Arnica Boost Recovery 946 mL in 1 TUBE GEL 946 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75638-009 DOCTOR HOYS ARNICA BOOST RECOVERY (ARNICA MONTANA) GEL [DYNAMIC BLENDING SPECIALISTS, INC.] 2 Current NDC, 3 package rows 20250201_7e639152-b423-4db8-9078-b5c929d6a07d.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 1 of 1 · 1 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 75638-009-00 75638000900 89 mL in 1 TUBE (75638-009-00) 89 ml 2023-03-01 2028-01-24 No No Historical 75638-009-01 75638000901 177 mL in 1 TUBE (75638-009-01) 177 ml 2023-03-01 2028-01-24 No No Historical 75638-009-02 75638000902 946 mL in 1 TUBE (75638-009-02) 946 ml 2023-03-01 2028-04-17 No No Historical