NDC 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

NDC Product Code 51885-9489

NDC CODE: 51885-9489

Proprietary Name: Zeel What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary 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 What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 51885 - Biologische Heilmittel Heel

NDC 51885-9489-8

Package Description: 1 TUBE in 1 CARTON > 100 g in 1 TUBE

NDC Product Information

Zeel with NDC 51885-9489 is a a human over the counter drug product labeled by Biologische Heilmittel Heel. The generic name of Zeel is 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. The product's dosage form is ointment and is administered via topical form.

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Zeel Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Biologische Heilmittel Heel
Labeler Code: 51885
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-22-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Zeel Product Label Images

Zeel Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index


Warnings: For external use only. Do not use ifpregnant or breast-feeding. Do not apply over openwounds or broken skin. In rare cases, allergic skin reactionsmay develop. Keep out of reach of children. Ifsymptoms persist or worsen a healthcare provider should beconsulted. If swallowed, get medical help or contact aPoison Control Center right away. Do not use if knownsensitivity to Zeel® or any of its ingredients exists.


Directions: Adults: Apply generously to affected areas2 to 3 times daily, or as directed by your health professional.Massage thoroughly into skin. Children under 18 yearsof age: consult your healthcare professional.Indications: For the temporary relief of minor arthritispain and joint stiffness

Inactive Ingredients:

Inactive ingredients:Cetostearyl alcohol, Paraffin, Ethanol, Puriffied water, White Petrolatum

Keep Out Of Reach Of Children



Indications: For the temporary relief of minor arthritis pain and joint stuffness.


Arthritis Pain Relief

Active Ingrendent

Active ingredients: Each 100 g contains: _-Lipoicum acidum6X 0.01g, *Arnica montana, radix 2X 0.3g, *Cartilago suis 2X0.001g (Final concentration 7X), Coenzyme A 6X 0.01g, *Dulcamara2X 0.08g, *Embryo suis 2X 0.001g (Final concentration 7X),*Funiculus umbilicalis suis 2X 0.001g (Final concentration 7X)Nadidum 6X 0.01g, Natrum oxalaceticum 6X 0.01g, *Placentatotalis suis 2X 0.001g (Final concentration 7X), *Rhus toxicodendron2X 0.27g (Final concentration 4X), *Sanguinaria canadensis 2X0.23g (Final concentration 4X), *Silicea 6X 1g, *Sulphur 6X 0.27g,*Symphytum officinale 8X 0.75g. *Natural Ingredient

* Please review the disclaimer below.