NDC 63083-1001 Pets 1001
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-1001?
What are the uses for Pets 1001?
Which are Pets 1001 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- CAMELUS BACTRIANUS HAIR (UNII: T94T602XJN)
- CAMELUS BACTRIANUS HAIR (UNII: T94T602XJN) (Active Moiety)
- FELIS CATUS HAIR (UNII: 1564HD0N96)
- FELIS CATUS HAIR (UNII: 1564HD0N96) (Active Moiety)
- BOVINE TYPE I COLLAGEN (SKIN) (UNII: 0127KU7397)
- BOVINE TYPE I COLLAGEN (SKIN) (UNII: 0127KU7397) (Active Moiety)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (Active Moiety)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (Active Moiety)
- BLUEGILL (UNII: 4B28FOZ5UQ)
- BLUEGILL (UNII: 4B28FOZ5UQ) (Active Moiety)
- CAPRA HIRCUS HAIR (UNII: 16M9MK8C4W)
- CAPRA HIRCUS HAIR (UNII: 16M9MK8C4W) (Active Moiety)
- CAVIA PORCELLUS WHOLE (UNII: XJI597GH9P)
- CAVIA PORCELLUS WHOLE (UNII: XJI597GH9P) (Active Moiety)
- SUS SCROFA HAIR (UNII: 7Q7T9Z7QUW)
- SUS SCROFA HAIR (UNII: 7Q7T9Z7QUW) (Active Moiety)
- HORSE (UNII: 2218S6BEDD)
- HORSE (UNII: 2218S6BEDD) (Active Moiety)
- RABBIT (UNII: O5V0F26RUW)
- RABBIT (UNII: O5V0F26RUW) (Active Moiety)
- SHEEP WOOL (UNII: 503LYG631H)
- SHEEP WOOL (UNII: 503LYG631H) (Active Moiety)
Which are Pets 1001 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".