NDC 55030-003 Blackcurrantenzymepowder
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55030 - Shenzhen Aiwei Biological Technology Co., Ltd.
- 55030-003 - Blackcurrantenzymepowder
Product Characteristics
Product Packages
NDC Code 55030-003-02
Package Description: 15 PACKAGE in 1 PACKAGE, COMBINATION / 3 g in 1 PACKAGE (55030-003-01)
Product Details
What is NDC 55030-003?
What are the uses for Blackcurrantenzymepowder?
Which are Blackcurrantenzymepowder UNII Codes?
The UNII codes for the active ingredients in this product are:
- .BETA.-CAROTENE (UNII: 01YAE03M7J)
- .BETA.-CAROTENE (UNII: 01YAE03M7J) (Active Moiety)
- KERACYANIN (UNII: V0N2VMB4FV)
- KERACYANIN (UNII: V0N2VMB4FV) (Active Moiety)
- LUTEIN (UNII: X72A60C9MT)
- LUTEIN (UNII: X72A60C9MT) (Active Moiety)
- .BETA.-CAROTENE, (9Z)- (UNII: 3K5NFW97PV)
- .BETA.-CAROTENE, (9Z)- (UNII: 3K5NFW97PV) (Active Moiety)
- STRAWBERRY (UNII: 4J2TY8Y81V)
- STRAWBERRY (UNII: 4J2TY8Y81V) (Active Moiety)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- MALTODEXTRIN (UNII: 7CVR7L4A2D) (Active Moiety)
- CRANBERRY (UNII: 0MVO31Q3QS)
- CRANBERRY (UNII: 0MVO31Q3QS) (Active Moiety)
Which are Blackcurrantenzymepowder 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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[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".