NDC 71497-030 Labno 4sp Safe Bright Tone Bb Cushion
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71497 - Kb Lab Co., Ltd.
- 71497-030 - Labno 4sp Safe Bright Tone Bb Cushion
Product Packages
NDC Code 71497-030-02
Package Description: 1 CONTAINER in 1 CARTON / 14 g in 1 CONTAINER (71497-030-01)
Product Details
What is NDC 71497-030?
What are the uses for Labno 4sp Safe Bright Tone Bb Cushion?
Which are Labno 4sp Safe Bright Tone Bb Cushion UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Labno 4sp Safe Bright Tone Bb Cushion 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:
- WATER (UNII: 059QF0KO0R)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
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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".