NDC 70223-001 Elroselabs
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 70223-001?
What are the uses for Elroselabs?
Which are Elroselabs UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- POTASSIUM BROMIDE (UNII: OSD78555ZM)
- BROMIDE ION (UNII: 952902IX06) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
Which are Elroselabs 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:
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- CLOVE OIL (UNII: 578389D6D0)
- CEDRUS ATLANTICA BARK OIL (UNII: ZX5QRE4U60)
- OREGANO LEAF OIL (UNII: 7D0CGR40U1)
- NIAOULI OIL (UNII: D50IC2T8FU)
- COCONUT OIL (UNII: Q9L0O73W7L)
- WHITE WAX (UNII: 7G1J5DA97F)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- GLYCERIN (UNII: PDC6A3C0OX)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- TEA TREE OIL (UNII: VIF565UC2G)
- MELISSA OFFICINALIS (UNII: YF70189L0N)
- CROTON LECHLERI RESIN (UNII: GGG6W25C63)
- EUCALYPTUS CAMALDULENSIS LEAF OIL (UNII: SN6D1J15I6)
* 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".