NDC 63083-9203 Aletris Combination 9203
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-9203 - Aletris Combination
Product Packages
NDC Code 63083-9203-1
Package Description: 29.5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-9203?
What are the uses for Aletris Combination 9203?
Which are Aletris Combination 9203 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALETRIS FARINOSA ROOT (UNII: O021JGR97X)
- ALETRIS FARINOSA ROOT (UNII: O021JGR97X) (Active Moiety)
- ANAMIRTA COCCULUS FRUIT (UNII: 3E8XBL6YYK)
- ANAMIRTA COCCULUS FRUIT (UNII: 3E8XBL6YYK) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- FERRIC CATION (UNII: 91O4LML611)
- FERRIC CATION (UNII: 91O4LML611) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- FERROUS CATION (UNII: GW89581OWR)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
- CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U)
- CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- PICRIC ACID (UNII: A49OS0F91S)
- PICRIC ACID (UNII: A49OS0F91S) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- QUININE ARSENITE (UNII: 42QO5P0NLM)
- QUININE (UNII: A7V27PHC7A) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
Which are Aletris Combination 9203 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".