NDC 60512-8027 Natrum Muriaticum

NDC Product Code 60512-8027

NDC CODE: 60512-8027

Proprietary Name: Natrum Muriaticum 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.

NDC Code Structure

NDC 60512-8027-5

Package Description: 125 TABLET, CHEWABLE in 1 JAR

NDC 60512-8027-6

Package Description: 500 TABLET, CHEWABLE in 1 JAR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Natrum Muriaticum with NDC 60512-8027 is a product labeled by Homeolab Usa Inc. The product's dosage form is and is administered via form.

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.


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
Start Marketing Date: 03-20-2014 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Natrum Muriaticum 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

Natrum muriaticum (Sodium chloride) 6X


...........................................Water retention, hay fever, colds, constipation


The letters 'HPUS' indicate that the component in this product is officially monographed in the Homoeopathic Pharmacopoeia of the United States.


This tissue salt helps relieve symptoms associated with water retention in women, hay fever and colds with watery discharge and constipation.**These claims have not been reviewed by the Food and Drug Administration. They are based on traditional homeopathic practice.

Otc - Stop Use

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

Otc - Pregnancy Or Breast Feeding

As with any drug, ask a doctor before use if pregnant or nursing.

Otc - Keep Out Of Reach Of Children

Keep this and all medications out of the reach of children.In case of emergency or accidental overdose, contact a medical professional or a Poison Control Center immediately.


Children from 2 to 5 years: Crush 2 tablets and dissolve in water 3 times daily, or as directed by a healthcare professional.Adults and children over 5 years: Chew 2 tablets 3 times daily, or as directed by a healthcare professional.• Do not use more than directed.• Do not take with food.

Other Information

Store at room temperature.Do not use if cap seal is broken or missing.

Inactive Ingredients

Lactose, magnesium stearate.

* Please review the disclaimer below.