NDC 63083-7001 Ret Stomach 7001
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-7001 - Ret Stomach
Product Packages
NDC Code 63083-7001-1
Package Description: 29.5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-7001?
What are the uses for Ret Stomach 7001?
Which are Ret Stomach 7001 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89)
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89) (Active Moiety)
- MALUS SYLVESTRIS FLOWER (UNII: 6ZJ8N1924Z)
- MALUS SYLVESTRIS FLOWER (UNII: 6ZJ8N1924Z) (Active Moiety)
- IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
- IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
- SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R)
- SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- PULSATILLA MONTANA WHOLE (UNII: 24K790T39B)
- PULSATILLA MONTANA WHOLE (UNII: 24K790T39B) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Ret Stomach 7001 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)
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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".