NDC 54118-7976 Aller-tox 1
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 54118-7976?
What are the uses for Aller-tox 1?
Which are Aller-tox 1 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETALDEHYDE (UNII: GO1N1ZPR3B)
- ACETALDEHYDE (UNII: GO1N1ZPR3B) (Active Moiety)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- CORTISONE (UNII: V27W9254FZ)
- CORTISONE (UNII: V27W9254FZ) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- GALLIC ACID MONOHYDRATE (UNII: 48339473OT)
- GALLIC ACID (UNII: 632XD903SP) (Active Moiety)
- HISTAMINE (UNII: 820484N8I3)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- HYALURONIDASE (UNII: 8KOG53Z5EM)
- HYALURONIDASE (UNII: 8KOG53Z5EM) (Active Moiety)
- INTERFERON BETA-1A (UNII: XRO4566Q4R)
- INTERFERON BETA-1A (UNII: XRO4566Q4R) (Active Moiety)
- MAMMAL LIVER (UNII: D0846624BI)
- MAMMAL LIVER (UNII: D0846624BI) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- BOS TAURUS MESENCHYME (UNII: 3802H34QRI)
- BOS TAURUS MESENCHYME (UNII: 3802H34QRI) (Active Moiety)
- SEROTONIN (UNII: 333DO1RDJY)
- SEROTONIN (UNII: 333DO1RDJY) (Active Moiety)
- HYDRANGEA ARBORESCENS ROOT (UNII: SFK828Q2DE)
- HYDRANGEA ARBORESCENS ROOT (UNII: SFK828Q2DE) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
Which are Aller-tox 1 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- 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".