NDC 17312-020 Chronic Fatigue Therapy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 17312-020?
What are the uses for Chronic Fatigue Therapy?
Which are Chronic Fatigue Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K)
- HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K) (Active Moiety)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- INFLUENZA B VIRUS (UNII: 1314JZ2X6W)
- INFLUENZA B VIRUS (UNII: 1314JZ2X6W) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- SCUTELLARIA LATERIFLORA TOP (UNII: C6CNB75R61)
- SCUTELLARIA LATERIFLORA TOP (UNII: C6CNB75R61) (Active Moiety)
Which are Chronic Fatigue Therapy 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:
- MANNITOL (UNII: 3OWL53L36A)
- SORBITOL (UNII: 506T60A25R)
- CROSPOVIDONE (UNII: 68401960MK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- COPOVIDONE (UNII: D9C330MD8B)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
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[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".