NDC 35378-0002 Boost Remedy Water

NDC Product Code 35378-0002

NDC 35378-0002-2

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

NDC 35378-0002-3

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

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

NDC Product Information

Boost Remedy Water with NDC 35378-0002 is a product labeled by Georgetown Health, Llc Dba Essentialife. The generic name of Boost Remedy Water is . The product's dosage form is and is administered via form.

Labeler Name: Georgetown Health, Llc Dba Essentialife

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.

  • SUCROSE (UNII: C151H8M554)

Product Labeler Information

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

Labeler Name: Georgetown Health, Llc Dba Essentialife
Labeler Code: 35378
Start Marketing Date: 07-01-2012 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: 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.

Boost Remedy Water Product Label Images

Boost Remedy Water 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

Adrenalinum15xAloe socotrina15xArsenicum album15xBaptisia tinctoria15xBerberis aquifolium15xBerberis vulgaris15xBryonia 15xChelidonium majus15xCrotalus horridus15xDigitalis purpurea15xFerrum metallicum15xGlonoinum15xGlycyrrhiza glabra15xHydrocotyle asiatica15xIodium15xIris versicolor15xLachesis mutus15xLycopodium clavatum15xNatrum muriaticum15xNux vomica15xRhus toxicodendron15xRuta graveolens15xThuja occidentalis15xThyroidinum15xEchinacea   3xLappa major   3xSolidago virgaurea  3xTaraxacum officinale  3x


Formulated for symptoms associated with low energy, mild stress and weakness.


Formulated for symptoms associated with low energy, mild stress and weakness.


Do not use if tamper-evident package seal is broken or missing.  Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.  Keep out of reach of children.


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.

Inactive Ingredients

USP/NF neutral pellets (.07% gluten-free, non-GMO, beet-derived sucrose, .03% gluten-free, non-GMO maize starch in 500 ml water)

Other Information

Avoid storing where temperatures may exceed 140 degrees.



* Please review the disclaimer below.