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