NDC 63083-1023 Smoke Mix 1023
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-1023 - Smoke Mix
Product Packages
NDC Code 63083-1023-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-1023?
What are the uses for Smoke Mix 1023?
Which are Smoke Mix 1023 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- ALOE SPICATA WHOLE (UNII: 053IJC048X)
- ALOE SPICATA WHOLE (UNII: 053IJC048X) (Active Moiety)
- TOBACCO SMOKE (UNII: 9BPR10844H)
- TOBACCO SMOKE (UNII: 9BPR10844H) (Active Moiety)
- LIQUID PETROLEUM (UNII: 6ZAE7X688J)
- LIQUID PETROLEUM (UNII: 6ZAE7X688J) (Active Moiety)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN) (Active Moiety)
- GUTTA PERCHA (UNII: 6Z9BZ8Q1D0)
- GUTTA PERCHA (UNII: 6Z9BZ8Q1D0) (Active Moiety)
- TABTOXIN (UNII: H3YX70R64N)
- TABTOXIN (UNII: H3YX70R64N) (Active Moiety)
Which are Smoke Mix 1023 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)
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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".