NDC 36987-1334 Honeydew Melon
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 36987-1334?
What are the uses for Honeydew Melon?
Which are Honeydew Melon 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)
Which are Honeydew Melon 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)
What is the NDC to RxNorm Crosswalk for Honeydew Melon?
- RxCUI: 1000013 - whole wheat allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 1000013 - whole wheat allergenic extract 0.05 GM/ML Injectable Solution
- RxCUI: 1000013 - whole wheat extract 50 MG/ML Injectable Solution
- RxCUI: 1006513 - barley malt allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 1006513 - barley (malt) allergenic extract 0.05 GM/ML Injectable Solution
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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".