NDC 63083-7012 Ret Pituitary/sex 7012
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-7012 - Ret Pituitary/sex
Product Packages
NDC Code 63083-7012-1
Package Description: 29.5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-7012?
What are the uses for Ret Pituitary/sex 7012?
Which are Ret Pituitary/sex 7012 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89)
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89) (Active Moiety)
- VITIS VINIFERA FLOWERING TOP (UNII: 6TG3V35HTV)
- VITIS VINIFERA FLOWERING TOP (UNII: 6TG3V35HTV) (Active Moiety)
- ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q)
- ROSA CANINA FLOWER (UNII: 81MCR2UQ6Q) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- CINCHONA BARK (UNII: 292E43P4I9)
- CINCHONA BARK (UNII: 292E43P4I9) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- 1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOCHOLINE (UNII: 043IPI2M0K)
- 1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOCHOLINE (UNII: 043IPI2M0K) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
Which are Ret Pituitary/sex 7012 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".