NDC 71631-0004 37.4

Water

NDC Product Code 71631-0004

NDC Product Information

37.4 with NDC 71631-0004 is a a human over the counter drug product labeled by Jesus Glory Bio Co.,ltd.. The generic name of 37.4 is water. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Jesus Glory Bio Co.,ltd.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

37.4 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.

  • WATER 99.9974 g/100L

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.

  • OXYGEN (UNII: S88TT14065)

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: Jesus Glory Bio Co.,ltd.
Labeler Code: 71631
Marketing Category: UNAPPROVED DRUG OTHER - 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: 07-18-2019 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: 12-31-2020 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.

37.4 Product Label Images

37.4 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

Otc - Active Ingredient

Water

Inactive Ingredient

Oxygen

Otc - Purpose

To help the treatment and prevention of blood circulation, antioxidant

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Take 100ml each time

Warnings

Avoid direct sunlight and store in a cool place.

Zone Due to the nature of the product containing oxygen, the container may be damaged if it is frozen (stored frozen).

Be careful because if you shake too hard or apply heat, the lid may open.

Dosage & Administration

For oral use only

* Please review the disclaimer below.

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