NDC 63083-2030 Hypotonia Drops 2030
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2030 - Hypotonia Drops
Product Packages
NDC Code 63083-2030-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2030?
What are the uses for Hypotonia Drops 2030?
Which are Hypotonia Drops 2030 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36)
- HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (Active Moiety)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- ASIAN GINSENG (UNII: CUQ3A77YXI) (Active Moiety)
- CYTISUS SCOPARIUS FLOWERING TOP (UNII: XZC6H8R666)
- CYTISUS SCOPARIUS FLOWERING TOP (UNII: XZC6H8R666) (Active Moiety)
- PRUNUS LAUROCERASUS LEAF (UNII: F26P2D4757)
- PRUNUS LAUROCERASUS LEAF (UNII: F26P2D4757) (Active Moiety)
- NERIUM OLEANDER WHOLE (UNII: JG9V5H8412)
- NERIUM OLEANDER WHOLE (UNII: JG9V5H8412) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- BEEF KIDNEY (UNII: 5HOC10FSIC)
- BEEF KIDNEY (UNII: 5HOC10FSIC) (Active Moiety)
- ANGIOTENSIN I (UNII: 9C880YQG7C)
- ANGIOTENSIN I (UNII: 9C880YQG7C) (Active Moiety)
Which are Hypotonia Drops 2030 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* Please review the disclaimer below.
[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".