Home NDC 51885-9489 Zeel
Product NDC 51885-9489
11-digit product format 518859489
Labeler code 51885
Product ID 51885-9489_49ef1c5d-a07b-4bc0-9de1-dc40d8477d8f
Type HUMAN OTC DRUG
Nonproprietary name ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER
Dosage form OINTMENT
Route TOPICAL
Labeler Biologische Heilmittel Heel
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-09-22
Substance ALPHA LIPOIC ACID; ARNICA MONTANA WHOLE; COENZYME A; CORIANDER; NADIDE; SANGUINARIA CANADENSIS ROOT; SILICON DIOXIDE; SODIUM DIETHYL OXALACETATE; SOLANUM DULCAMARA TOP; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA EMBRYO; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; TOXICODENDRON PUBESCENS LEAF
Active strength 6; 2; 6; 8; 6; 2; 6; 6; 2; 6; 2; 2; 2; 2; 2 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Zeel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALPHA LIPOIC ACID 6 [hp_X]/g ARNICA MONTANA WHOLE 2 [hp_X]/g SUS SCROFA CARTILAGE 6 [hp_X]/g COENZYME A 8 [hp_X]/g SOLANUM DULCAMARA TOP 6 [hp_X]/g SUS SCROFA EMBRYO 2 [hp_X]/g SUS SCROFA UMBILICAL CORD 6 [hp_X]/g NADIDE 6 [hp_X]/g SODIUM DIETHYL OXALACETATE 2 [hp_X]/g SUS SCROFA PLACENTA 6 [hp_X]/g TOXICODENDRON PUBESCENS LEAF 2 [hp_X]/g SANGUINARIA CANADENSIS ROOT 2 [hp_X]/g SILICON DIOXIDE 2 [hp_X]/g SULFUR 2 [hp_X]/g CORIANDER 2 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 15 matching rows.
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 51885-9489-8 Zeel 1 in 1 CARTON OINTMENT 1 3 51885-9489-8 Zeel 100 g in 1 TUBE OINTMENT 100 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51885-9489 ZEEL (ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER) OINTMENT [BIOLOGISCHE HEILMITTEL HEEL] 3 Current NDC, Legacy NDC, 2 package rows 20230929_d5d7a2e5-a6ce-4a41-9430-1378023aa7d0.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Zeel ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER Biologische Heilmittel Heel d5d7a2e5-a6ce-4a41-9430-1378023aa7d0 2023-09-28 Warnings Exact identifier ndc (product): 51885-9489
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 51885-9489-8 51885948908 1 TUBE in 1 CARTON (51885-9489-8) / 100 g in 1 TUBE 1 tube 2021-09-22 0000-00-00 No No Current