NDC 63083-2001 Acne Drops 2001
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2001 - Acne Drops
Product Packages
NDC Code 63083-2001-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2001?
What are the uses for Acne Drops 2001?
Which are Acne Drops 2001 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARCTIUM LAPPA ROOT OIL (UNII: 55DGS3F5YG)
- ARCTIUM LAPPA ROOT OIL (UNII: 55DGS3F5YG) (Active Moiety)
- BERBERIS AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB)
- BERBERIS AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB) (Active Moiety)
- CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
- CENTELLA ASIATICA LEAF (UNII: 6810070TYD) (Active Moiety)
- RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P)
- RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
- POTASSIUM BROMIDE (UNII: OSD78555ZM)
- BROMIDE ION (UNII: 952902IX06) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- CARBO ANIMALIS (UNII: 279O8I0433)
- CARBO ANIMALIS (UNII: 279O8I0433) (Active Moiety)
Which are Acne Drops 2001 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".