NDC 57520-0527 Endo Pure Testos (for Women)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0527 - Endo Pure Testos (for Women)
Product Packages
NDC Code 57520-0527-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57520-0527?
What are the uses for Endo Pure Testos (for Women)?
Which are Endo Pure Testos (for Women) UNII Codes?
The UNII codes for the active ingredients in this product are:
- SAW PALMETTO (UNII: J7WWH9M8QS)
- SAW PALMETTO (UNII: J7WWH9M8QS) (Active Moiety)
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (Active Moiety)
- TESTOSTERONE (UNII: 3XMK78S47O)
- TESTOSTERONE (UNII: 3XMK78S47O) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (Active Moiety)
- HERRING SPERM DNA (UNII: 51FI676N6F)
- HERRING SPERM DNA (UNII: 51FI676N6F) (Active Moiety)
Which are Endo Pure Testos (for Women) 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* 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".