NDC 54973-3122 Bioplasma Sport With Electrolytes

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:
54973-3122
Proprietary Name:
Bioplasma Sport With Electrolytes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
54973
Start Marketing Date: [9]
04-06-2011
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
CITRUS (C73378)

Code Structure Chart

Product Details

What is NDC 54973-3122?

The NDC code 54973-3122 is assigned by the FDA to the product Bioplasma Sport With Electrolytes which is product labeled by Hyland's. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54973-3122-2 12 packet in 1 carton / 2 g in 1 packet (54973-3122-1). 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 Bioplasma Sport With Electrolytes?

Adults and children 7-12 years: Pour 1 packet directly on tongue without tilting head or inhaling. Close mouth. Powder will dissolve quickly. Each single-dose packet can also be dissolved into an 8 oz glass or bottle of water. Stir or shake to dissolve powder. Water may be sipped throughout activity. For best results, repeat every 3-4 hours as needed, before during or after activity. Children Ages 2-6 years: One-Half adult dose (packet).

Which are Bioplasma Sport With Electrolytes UNII Codes?

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

Which are Bioplasma Sport With Electrolytes 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".