NDC 35378-0004 Calm Remedy Water

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
35378-0004
Proprietary Name:
Calm Remedy Water
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Georgetown Health, Llc Dba Essentialife
Labeler Code:
35378
Start Marketing Date: [9]
07-01-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
1 MM
Score:
1

Product Packages

NDC Code 35378-0004-2

Package Description: 7 CYLINDER in 1 CONTAINER / 1000 mg in 1 CYLINDER

NDC Code 35378-0004-3

Package Description: 1 CYLINDER in 1 CONTAINER / 1000 mg in 1 CYLINDER

Product Details

What is NDC 35378-0004?

The NDC code 35378-0004 is assigned by the FDA to the product Calm Remedy Water which is product labeled by Georgetown Health, Llc Dba Essentialife. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 35378-0004-2 7 cylinder in 1 container / 1000 mg in 1 cylinder, 35378-0004-3 1 cylinder in 1 container / 1000 mg in 1 cylinder. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Calm Remedy Water?

Ages 12 and up. Remedy Water® homepathic pellets are dispersed via the PowerCap® apparatus. Firmly press PowerCap® dome to release pellets into the bottle of water and shake well. Remedy Water® pellets may not dissolve completely. Drink within four hours. Avoid storing or washing where temperatures may exceed 140 degrees.

Which are Calm Remedy Water UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Calm Remedy Water Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".