Home NDC 43689-0070 DB Foot Pain Relieving
Product NDC 43689-0070
11-digit product format 436890070
Labeler code 43689
Product ID 43689-0070_52b905b2-0678-bf51-e063-6294a90a3d11
Type HUMAN OTC DRUG
Nonproprietary name Apis Mellifica, Gelsemium Sempervirens, Gnaphalium
Dosage form SPRAY
Route TOPICAL
Labeler The Magni Company
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-12-01
Substance APIS MELLIFERA; GELSEMIUM SEMPERVIRENS WHOLE; PSEUDOGNAPHALIUM LUTEOALBUM LEAF
Active strength 3; 6; 3 [hp_X]/100g; [hp_X]/100g; [hp_X]/100g
Pharmacologic classes Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
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 DB Foot Pain Relieving
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PSEUDOGNAPHALIUM LUTEOALBUM LEAF 3 [hp_X]/100g GELSEMIUM SEMPERVIRENS WHOLE 6 [hp_X]/100g APIS MELLIFERA 3 [hp_X]/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination BGI20Z6M57 Internal UNII lookup R0519OZO3K Internal UNII lookup 7S82P3R43Z 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 43689-0070-3 DB Foot Pain Relieving 85 g in 1 BOTTLE, SPRAY SPRAY 85 2
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 Sample Exclude flag Status 43689-0070-3 43689007003 85 g in 1 BOTTLE, SPRAY (43689-0070-3) 85 g 2025-12-01 No No Current