NDC 63083-2121 Distress Drops 2121
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-2121?
What are the uses for Distress Drops 2121?
Which are Distress Drops 2121 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- FERULA ASSA-FOETIDA RESIN (UNII: W9FZA51AS1)
- FERULA ASSA-FOETIDA RESIN (UNII: W9FZA51AS1) (Active Moiety)
- DICENTRA CANADENSIS ROOT (UNII: Y5JS7YM46F)
- DICENTRA CANADENSIS ROOT (UNII: Y5JS7YM46F) (Active Moiety)
- HYOSCYAMUS NIGER (UNII: 4WRK2153H3)
- HYOSCYAMUS NIGER (UNII: 4WRK2153H3) (Active Moiety)
- FERULA SUMBUL ROOT (UNII: GLA4808EHQ)
- FERULA SUMBUL ROOT (UNII: GLA4808EHQ) (Active Moiety)
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
- CICUTA VIROSA WHOLE (UNII: 3E698BL84C)
- CICUTA VIROSA WHOLE (UNII: 3E698BL84C) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- GAULTHERIA PROCUMBENS TOP (UNII: 830295X963)
- GAULTHERIA PROCUMBENS TOP (UNII: 830295X963) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
Which are Distress Drops 2121 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)
* 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".