NDC 57520-0473 Hcgdelivery Com
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0473 - Hcgdelivery Com
Product Packages
NDC Code 57520-0473-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57520-0473?
What are the uses for Hcgdelivery Com?
Which are Hcgdelivery Com UNII Codes?
The UNII codes for the active ingredients in this product are:
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC ANHYDROUS (UNII: 22ADO53M6F)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB)
- HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB) (Active Moiety)
Which are Hcgdelivery Com 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- 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".