NDC 63083-2051 Abdominal Pain Drops 2051
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-2051?
What are the uses for Abdominal Pain Drops 2051?
Which are Abdominal Pain Drops 2051 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW)
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- BOS TAURUS SOLAR PLEXUS (UNII: Y8H8S1X8IB)
- BOS TAURUS SOLAR PLEXUS (UNII: Y8H8S1X8IB) (Active Moiety)
- TRIPE (UNII: C46FS57S0X)
- TRIPE (UNII: C46FS57S0X) (Active Moiety)
- SUS SCROFA PARASYMPATHETIC NERVE (UNII: 5AZZ2GHR69)
- SUS SCROFA PARASYMPATHETIC NERVE (UNII: 5AZZ2GHR69) (Active Moiety)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- HYDROCHLORIC ACID (UNII: QTT17582CB) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
Which are Abdominal Pain Drops 2051 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".