NDC 65692-0305 Vanilla Spf 15 Lip
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65692 - Raining Rose, Inc.
- 65692-0305 - Vanilla Spf 15 Lip
Product Characteristics
POMEGRANATE (C73411 - POMEGRANATE)
TROPICAL FRUIT PUNCH (C73419 - TROPICAL)
Product Packages
NDC Code 65692-0305-1
Package Description: 4.25 g in 1 PACKAGE
Product Details
What is NDC 65692-0305?
What are the uses for Vanilla Spf 15 Lip?
Which are Vanilla Spf 15 Lip 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Vanilla Spf 15 Lip 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:
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- SPEARMINT (UNII: J7I2T6IV1N)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- ROSEMARY (UNII: IJ67X351P9)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
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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".