NDC 62191-412 Protective Foundation Sunscreen Spf 15 412 Natural Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62191 - Sunrider Manufacturing L.p.
- 62191-412 - Protective Foundation Sunscreen Spf 15
Product Packages
NDC Code 62191-412-04
Package Description: 1 TUBE in 1 PACKAGE / 30 g in 1 TUBE
Product Details
What is NDC 62191-412?
What are the uses for Protective Foundation Sunscreen Spf 15 412 Natural Beige?
Which are Protective Foundation Sunscreen Spf 15 412 Natural Beige 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 Protective Foundation Sunscreen Spf 15 412 Natural Beige 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)
- ALMOND OIL (UNII: 66YXD4DKO9)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- GLYCERETH-26 (UNII: NNE56F2N14)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- KAOLIN (UNII: 24H4NWX5CO)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- OLETH-20 (UNII: YTH167I2AG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- SQUALENE (UNII: 7QWM220FJH)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TRICAPRIN (UNII: O1PB8EU98M)
- TRICAPRYLIN (UNII: 6P92858988)
- TROLAMINE (UNII: 9O3K93S3TK)
- AHNFELTIOPSIS CONCINNA (UNII: SMF2K46G8D)
- CAPRYLIC/CAPRIC/PALMITIC/STEARIC TRIGLYCERIDE (UNII: ZF29F7IK5I)
- JOJOBA OIL (UNII: 724GKU717M)
- BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)
- CORN STARCH 3-E-DODECENYL SUCCINIC ANHYDRIDE MODIFIED (UNII: QG4MW19XYX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
* 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".