NDC 76119-5308 Mally Lip Defender
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76119 - Mallygirl, Llc
- 76119-5308 - Mally Lip Defender
Product Packages
NDC Code 76119-5308-1
Package Description: 1 TUBE, WITH APPLICATOR in 1 BOX / 3.5 g in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 76119-5308?
What are the uses for Mally Lip Defender?
Which are Mally Lip Defender 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 Mally Lip Defender 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:
- POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- OCTYLDECANOL (UNII: 07UG7TSU58)
- CANDELILLA WAX (UNII: WL0328HX19)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- HYALURONIC ACID (UNII: S270N0TRQY)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MICA (UNII: V8A1AW0880)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 6 (UNII: 481744AI4O)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
* 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".