NDC 36987-1413 Broccoli
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 36987-1413?
What are the uses for Broccoli?
Which are Broccoli UNII Codes?
The UNII codes for the active ingredients in this product are:
- APPLE (UNII: B423VGH5S9)
- APPLE (UNII: B423VGH5S9) (Active Moiety)
- APRICOT (UNII: 269CJD5GZ9)
- APRICOT (UNII: 269CJD5GZ9) (Active Moiety)
- AVOCADO (UNII: SDS87L369F)
- AVOCADO (UNII: SDS87L369F) (Active Moiety)
- BANANA (UNII: 4AJZ4765R9)
- BANANA (UNII: 4AJZ4765R9) (Active Moiety)
- BLACKBERRY (UNII: 8A6OMU3I8L)
- BLACKBERRY (UNII: 8A6OMU3I8L) (Active Moiety)
- BLUEBERRY (UNII: 253RUG1X1A)
- BLUEBERRY (UNII: 253RUG1X1A) (Active Moiety)
- CANTALOUPE (UNII: 8QF5D5H6UH)
- CANTALOUPE (UNII: 8QF5D5H6UH) (Active Moiety)
- SOUR CHERRY (UNII: 1L29G6428X)
- SOUR CHERRY (UNII: 1L29G6428X) (Active Moiety)
- CRANBERRY (UNII: 0MVO31Q3QS)
- CRANBERRY (UNII: 0MVO31Q3QS) (Active Moiety)
- DATE (UNII: H3O7QI5HY7)
- DATE (UNII: H3O7QI5HY7) (Active Moiety)
- FIG (UNII: TGD87RII2U)
- FIG (UNII: TGD87RII2U) (Active Moiety)
- GRAPEFRUIT (UNII: O82C39RR8C)
- GRAPEFRUIT (UNII: O82C39RR8C) (Active Moiety)
- HONEYDEW MELON (UNII: RN8P45F92A)
- HONEYDEW MELON (UNII: RN8P45F92A) (Active Moiety)
- LEMON (UNII: 24RS0A988O)
- LEMON (UNII: 24RS0A988O) (Active Moiety)
- LIME (CITRUS) (UNII: 8CZS546954)
- LIME (CITRUS) (UNII: 8CZS546954) (Active Moiety)
- ORANGE (UNII: 5EVU04N5QU)
- ORANGE (UNII: 5EVU04N5QU) (Active Moiety)
- PEACH (UNII: 3OKE88I3QG)
- PEACH (UNII: 3OKE88I3QG) (Active Moiety)
- PEAR (UNII: 2ZN8DWC0YF)
- PEAR (UNII: 2ZN8DWC0YF) (Active Moiety)
- PINEAPPLE (UNII: 2A88ZO081O)
- PINEAPPLE (UNII: 2A88ZO081O) (Active Moiety)
- PLUM (UNII: 67M3EQ6BE1)
- PLUM (UNII: 67M3EQ6BE1) (Active Moiety)
- RASPBERRY (UNII: 4N14V5R27W)
- RASPBERRY (UNII: 4N14V5R27W) (Active Moiety)
- STRAWBERRY (UNII: 4J2TY8Y81V)
- STRAWBERRY (UNII: 4J2TY8Y81V) (Active Moiety)
- TANGERINE (UNII: KH3E3096OO)
- TANGERINE (UNII: KH3E3096OO) (Active Moiety)
- WATERMELON (UNII: 231473QB6R)
- WATERMELON (UNII: 231473QB6R) (Active Moiety)
- ARTICHOKE (UNII: 4F3W47PLBE)
- ARTICHOKE (UNII: 4F3W47PLBE) (Active Moiety)
- ASPARAGUS (UNII: Z1EJP3037Z)
- ASPARAGUS (UNII: Z1EJP3037Z) (Active Moiety)
- KIDNEY BEAN (UNII: M98C8416QO)
- KIDNEY BEAN (UNII: M98C8416QO) (Active Moiety)
- LIMA BEAN (UNII: 112YH1ZMX2)
- LIMA BEAN (UNII: 112YH1ZMX2) (Active Moiety)
- STRING BEAN (UNII: N9D69B2Q7Y)
- STRING BEAN (UNII: N9D69B2Q7Y) (Active Moiety)
- BEET (UNII: N487KM8COK)
- BEET (UNII: N487KM8COK) (Active Moiety)
- BROCCOLI (UNII: UOI4FT57BZ)
- BROCCOLI (UNII: UOI4FT57BZ) (Active Moiety)
Which are Broccoli 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)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- PHENOL (UNII: 339NCG44TV)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Broccoli?
- RxCUI: 1006347 - arabica coffee bean allergenic extract 100 MG/ML Injectable Solution
- RxCUI: 1006347 - arabica coffee bean allergenic extract 0.1 GM/ML Injectable Solution
- RxCUI: 1010702 - blackberry allergenic extract 100 MG/ML Injectable Solution
- RxCUI: 1010702 - blackberry allergenic extract 0.1 GM/ML Injectable Solution
- RxCUI: 1010704 - blueberry allergenic extract 100 MG/ML Injectable Solution
* 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".