NDC 51770-001 Truth Revealed Super Creme Spf 15 Ole Henriksen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51770 - Ole Henriksen
- 51770-001 - Truth Revealed Super Creme Spf 15
Product Packages
NDC Code 51770-001-02
Package Description: 1 JAR in 1 PACKAGE / 50 g in 1 JAR (51770-001-01)
Product Details
What is NDC 51770-001?
What are the uses for Truth Revealed Super Creme Spf 15 Ole Henriksen?
Which are Truth Revealed Super Creme Spf 15 Ole Henriksen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Truth Revealed Super Creme Spf 15 Ole Henriksen 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- PULLULAN (UNII: 8ZQ0AYU1TT)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- PLUKENETIA VOLUBILIS SEED OIL (UNII: 8ED72Z8J1Z)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- CALCIUM ASCORBATE (UNII: 183E4W213W)
- CHAMOMILE (UNII: FGL3685T2X)
- CARROT (UNII: L56Z1JK48B)
- AVENA SATIVA LEAF (UNII: 206PI19V7R)
- VACCINIUM MYRTILLUS LEAF (UNII: Y4U591OU70)
- SUCROSE (UNII: C151H8M554)
- ACER SACCHARUM BARK/SAP (UNII: Z120VL0KAC)
- ORANGE (UNII: 5EVU04N5QU)
- LEMON (UNII: 24RS0A988O)
- LEVOMENOL (UNII: 24WE03BX2T)
- ALLANTOIN (UNII: 344S277G0Z)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CARBOMER 934 (UNII: Z135WT9208)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- PHYTIC ACID (UNII: 7IGF0S7R8I)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".