NDC 42221-0013 Mango Butter Lipstick Spf 10
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42221 - Art Cosmetics Srl
- 42221-0013 - Mango Butter Lipstick
Product Characteristics
BROWN (C48332 - NUDE)
PURPLE (C48327 - NATURAL PURPLE)
ORANGE (C48331 - ORANGE BROWN)
PINK (C48328 - FROST PINK)
PINK (C48328 - PINK)
PINK (C48328 - PEACH)
PURPLE (C48327 - PURPLE)
RED (C48326 - FUCHSIA)
ORANGE (C48331 - CORAL)
RED (C48326 - ORANGE RED)
BROWN (C48332 - NATURAL BROWN)
PINK (C48328 - ROSE)
Product Packages
NDC Code 42221-0013-1
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 100 g in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 42221-0013?
What are the uses for Mango Butter Lipstick Spf 10?
Which are Mango Butter Lipstick Spf 10 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Mango Butter Lipstick Spf 10 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:
- OCTYLDODECANOL (UNII: 461N1O614Y)
- CANDELILLA WAX (UNII: WL0328HX19)
- CERESIN (UNII: Q1LS2UJO3A)
- ANISYL ALCOHOL (UNII: 7N6XGV3U49)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- MANGO (UNII: I629I3NR86)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- MICA (UNII: V8A1AW0880)
- D&C RED NO. 6 (UNII: 481744AI4O)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
* 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".