NDC 62191-007 Protective Foundation Sunscreen Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62191-007?
What are the uses for Protective Foundation Sunscreen Spf 15?
Which are Protective Foundation Sunscreen Spf 15 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 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:
- 1-BUTENE (UNII: LY001N554L)
- AHNFELTIOPSIS CONCINNA (UNII: SMF2K46G8D)
- ALMOND OIL (UNII: 66YXD4DKO9)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- 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)
- WATER (UNII: 059QF0KO0R)
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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".