NDC 43772-0029 Hepatitis-sode
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43772 - Synergy Formulas, Inc.
- 43772-0029 - Hepatitis-sode
Product Packages
NDC Code 43772-0029-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43772-0029?
What are the uses for Hepatitis-sode?
Which are Hepatitis-sode UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRITICUM AESTIVUM WHOLE (UNII: 3C3Y389JBU)
- TRITICUM AESTIVUM WHOLE (UNII: 3C3Y389JBU) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- GLUTATHIONE (UNII: GAN16C9B8O)
- GLUTATHIONE (UNII: GAN16C9B8O) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L)
- SUS SCROFA LYMPH (UNII: 33A7VYU29L) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (Active Moiety)
- CHELONE GLABRA (UNII: 6G3UN932VF)
- CHELONE GLABRA (UNII: 6G3UN932VF) (Active Moiety)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T) (Active Moiety)
- HEPATITIS A VIRUS (UNII: G54MT8V18G)
- HEPATITIS A VIRUS (UNII: G54MT8V18G) (Active Moiety)
- HEPATITIS C VIRUS (UNII: QI56415283)
- HEPATITIS C VIRUS (UNII: QI56415283) (Active Moiety)
- HEPATITIS B VIRUS (UNII: 77H9EM77P7)
- HEPATITIS B VIRUS (UNII: 77H9EM77P7) (Active Moiety)
Which are Hepatitis-sode 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".