NDC 78975-506 Care 1
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78975 - Lauree Llc
- 78975-506 - Care 1
Product Characteristics
Product Packages
NDC Code 78975-506-01
Package Description: 59 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 78975-506?
What are the uses for Care 1?
Which are Care 1 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Care 1 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:
- HYDROXYPROPYL CELLULOSE (TYPE M) (UNII: U3JF91U133)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- 2-(1-CHLOROCYCLOPROPYL)-3-(2-CHLOROPHENYL)-1,2-PROPANEDIOL (UNII: SJ211700DZ)
- ALOE (UNII: V5VD430YW9)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- COCONUT (UNII: 3RT3536DHY)
- CYMBOPOGON CITRATUS LEAF (UNII: 06JMS448M5)
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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".