NDC 60512-6009 Eczema Real Relief

NDC Product Code 60512-6009

NDC 60512-6009-0

Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE

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

NDC Product Information

Eczema Real Relief with NDC 60512-6009 is a product labeled by Homeolab Usa Inc.. The generic name of Eczema Real Relief is . The product's dosage form is and is administered via form.

Labeler Name: Homeolab Usa Inc.

Dosage Form: -

Product Type: 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.

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.

  • LACTOSE (UNII: J2B2A4N98G)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)

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: 07-25-2012 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: 12-31-2018 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 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.

Eczema Real Relief Product Label Images

Eczema 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

Fumaria officinalis (Common fumitory) 6CNatrum muriaticum (Salt) 6CAgaricus muscarius (Fly agaric) 6CPetroleum (Rock-oil) 6CSepia (Sepia) 6CKali arsenicosum (Potassium arsenite) 6CAlumina (Alumina) 6C

References

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

Purpose

Dry scaly skindry and cracked skin, body rashitching and rednessintense itching behind the ears, redness, dry and cracked skinitchingdry skin and itchingitching rash

Uses

This homeopathic medicine helps relieve symptoms of eczema:- dry skin- body rashes- cracked skin- itching

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.

Directions

Chew tablets and let dissolve in mouth.Do not use more than directed.Do not take with food.Repeat 3 times daily and reduce intake with improvement or as directed by a health professional.AgeDoseAdults 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.