NDC 63083-9220 Crataegus Combination 9220
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-9220 - Crataegus Combination
Product Packages
NDC Code 63083-9220-1
Package Description: 29.5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-9220?
What are the uses for Crataegus Combination 9220?
Which are Crataegus Combination 9220 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36)
- HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (Active Moiety)
- SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- CASTOR FIBER SCENT GLAND SECRETION (UNII: 9X8XFD5ZQX)
- CASTOR FIBER SCENT GLAND SECRETION (UNII: 9X8XFD5ZQX) (Active Moiety)
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
- RANUNCULUS BULBOSUS WHOLE (UNII: AEQ8NXJ0MB)
- RANUNCULUS BULBOSUS WHOLE (UNII: AEQ8NXJ0MB) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Crataegus Combination 9220 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".