NDC 50114-6129 Spascupreel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50114 - Heel Inc
- 50114-6129 - Spascupreel
Product Packages
NDC Code 50114-6129-6
Package Description: 10 VIAL in 1 CARTON / 1.1 mL in 1 VIAL
Product Details
What is NDC 50114-6129?
What are the uses for Spascupreel?
Which are Spascupreel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- AMMONIUM BROMIDE (UNII: R0JB3224WS)
- AMMONIUM BROMIDE (UNII: R0JB3224WS) (Active Moiety)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
- CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
- ATROPINE SULFATE (UNII: 03J5ZE7KA5)
- SULFATE ION (UNII: 7IS9N8KPMG) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
- PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O)
- PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (Active Moiety)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
- AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037)
- AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
- CUPRIC SULFATE (UNII: LRX7AJ16DT)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
Which are Spascupreel 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
* 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".