Home NDC 43689-0062 Magnilife DB Pain Relieving Foot
Product NDC 43689-0062
11-digit product format 436890062
Labeler code 43689
Product ID 43689-0062_558fce1b-b7a9-b8c7-e063-6394a90aeab5
Type HUMAN OTC DRUG
Nonproprietary name APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR
Dosage form CREAM
Route TOPICAL
Labeler The Magni Group, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-06-29
Substance APIS MELLIFERA; LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE FLOWERING; SULFUR
Active strength 3; 6; 1 [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmacologic classes Allergens [CS], Allergens [CS], Bee Venoms [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC], 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 Magnilife DB Pain Relieving Foot
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength APIS MELLIFERA 3 [hp_X]/g LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE FLOWERING 6 [hp_X]/g SULFUR 1 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7S82P3R43Z Internal UNII lookup 7R4LQP52DM Internal UNII lookup 70FD1KFU70 Internal UNII 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 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 43689-0062-1 43689006201 113 g in 1 JAR (43689-0062-1) 113 g 2026-06-29 No No Current 43689-0062-2 43689006202 1 JAR in 1 BOTTLE, UNIT-DOSE (43689-0062-2) / 113 g in 1 JAR 1 jar 2026-06-29 No No Current