NDC 60512-6037 Indigestion Real Relief

Lycopodium Clavatum, Carduus Marianus, Chelidonium Majus, Boldo, Nux Vomica

NDC Product Code 60512-6037

NDC Code: 60512-6037

Proprietary Name: Indigestion Real Relief 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: Lycopodium Clavatum, Carduus Marianus, Chelidonium Majus, Boldo, Nux Vomica 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.

Product Characteristics

WHITE (C48325)
Shape: ROUND (C48348)
8 MM
Score: 1

NDC Code Structure

  • 60512 - Homeolab Usa Inc
    • 60512-6037 - Indigestion

NDC 60512-6037-0

Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE

NDC Product Information

Indigestion Real Relief with NDC 60512-6037 is a a human over the counter drug product labeled by Homeolab Usa Inc. The generic name of Indigestion Real Relief is lycopodium clavatum, carduus marianus, chelidonium majus, boldo, nux vomica. The product's dosage form is tablet, chewable and is administered via oral form.

Labeler Name: Homeolab Usa Inc

Dosage Form: Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.

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.

Indigestion Real Relief 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.


Administration Route(s)

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

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Homeolab Usa Inc
Labeler Code: 60512
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: 07-11-2012 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: 12-31-2019 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Indigestion Real Relief Product Label Images

Indigestion Real Relief 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

Active Ingredients Hpus

Lycopodium clavatum (Clubmoss) 8XCarduus marianus (Milk thistle) 8XChelidonium majus (Calandine) 8XBoldo (Chilean sassafras) 8XNux vomica (Poison nut) 8X


The letters 'HPUS' indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.


Heartburn, nauseaburping acidity, nauseaupset stomach, bilious vomitingslow digestion, digestion discomfortindigestion from overeating


This homeopathic medicine helps relieve symptoms associated with indigestion:- heartburn- upset stomach- digestive discomfort

Otc - Stop Use

Stop use and ask a doctor if symptoms worsen or persist for more than 7 days.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.


Chew tablets and let dissolve in mouth.Do not use more than directed.Do not take with food.Repeat 3 times daily and reduce with improvement or as directed by a health professional. Age DoseAdults and children 12 years of age and older2 tabletsChildren 2 to 11 years of age1 tabletChildren under 2 years of ageAsk a doctor

Other Information

Store at room temperature (68 - 77F).Do not use if seal is broken or missing.

Inactive Ingredients

Lactose, magnesium stearate.

* Please review the disclaimer below.

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