NDC 63083-9315 Simple Chlorinated Combination 9315
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What is NDC 63083-9315?
What are the uses for Simple Chlorinated Combination 9315?
Which are Simple Chlorinated Combination 9315 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN) (Active Moiety)
- CARBON TETRACHLORIDE (UNII: CL2T97X0V0)
- CARBON TETRACHLORIDE (UNII: CL2T97X0V0) (Active Moiety)
- CHLORINE (UNII: 4R7X1O2820)
- CHLORINE (UNII: 4R7X1O2820) (Active Moiety)
- CHLOROFORM (UNII: 7V31YC746X)
- CHLOROFORM (UNII: 7V31YC746X) (Active Moiety)
- ETHYLENE (UNII: 91GW059KN7)
- ETHYLENE (UNII: 91GW059KN7) (Active Moiety)
- BIS(2,4-DICHLOROBENZOYL) PEROXIDE (UNII: 0QC93Y0L96)
- BIS(2,4-DICHLOROBENZOYL) PEROXIDE (UNII: 0QC93Y0L96) (Active Moiety)
- HEXACHLOROPHENE (UNII: IWW5FV6NK2)
- HEXACHLOROPHENE (UNII: IWW5FV6NK2) (Active Moiety)
- TRICHLOROETHYLENE (UNII: 290YE8AR51)
- TRICHLOROETHYLENE (UNII: 290YE8AR51) (Active Moiety)
Which are Simple Chlorinated Combination 9315 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".