NDC 12027-209 Kiss Therapy Spf 30 Blueberry Lime Lip Balm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12027 - Marwins Beauty Products, Inc.
- 12027-209 - Kiss Therapy Spf 30 Blueberry Lime Lip Balm
Product Packages
NDC Code 12027-209-02
Package Description: 1 TUBE in 1 BLISTER PACK / 3.5 g in 1 TUBE (12027-209-01)
Product Details
What is NDC 12027-209?
Which are Kiss Therapy Spf 30 Blueberry Lime Lip Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Kiss Therapy Spf 30 Blueberry Lime Lip Balm 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:
- KONJAC MANNAN (UNII: 36W3E5TAMG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- JOJOBA OIL (UNII: 724GKU717M)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- MANDARIN OIL (UNII: NJO720F72R)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ACAI OIL (UNII: Z0W6766A2W)
- SYNTHETIC WAX (2900 MW) (UNII: U5UP035C8A)
- 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".