NDC 62673-164 Moisturizing Facial Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62673 - Neoteric Cosmetics, Inc.
- 62673-164 - Moisturizing Facial Sunscreen
Product Packages
NDC Code 62673-164-03
Package Description: 1 TUBE in 1 CARTON / 85 g in 1 TUBE
Product Details
What is NDC 62673-164?
What are the uses for Moisturizing Facial Sunscreen?
Which are Moisturizing Facial Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Moisturizing Facial Sunscreen 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- GLYCERYL DILAURATE (UNII: MFL3ZIE8SK)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW) (UNII: 997385V0VV)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TROLAMINE (UNII: 9O3K93S3TK)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
* 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".