NDC 71261-018 Jungsaemmool Skin Setting Tone-up Sun Base
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71261 - Jungsaemmool Beauty Co., Ltd.
- 71261-018 - Jungsaemmool Skin Setting Tone-up Sun Base
Product Packages
NDC Code 71261-018-02
Package Description: 1 CONTAINER in 1 CARTON / 40 mL in 1 CONTAINER (71261-018-01)
Product Details
What is NDC 71261-018?
What are the uses for Jungsaemmool Skin Setting Tone-up Sun Base?
Which are Jungsaemmool Skin Setting Tone-up Sun Base UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Jungsaemmool Skin Setting Tone-up Sun Base 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIBUTYL ADIPATE (UNII: F4K100DXP3)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- PEG-100 STEARATE (UNII: YD01N1999R)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYGLYCERYL-2 CAPRATE (UNII: JX7WXJ41DH)
- PANTHENOL (UNII: WV9CM0O67Z)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- MICA (UNII: V8A1AW0880)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SUCROSE STEARATE (UNII: 274KW0O50M)
- SQUALANE (UNII: GW89575KF9)
- JOJOBA OIL (UNII: 724GKU717M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
- ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
- HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PREZATIDE COPPER (UNII: 6BJQ43T1I9)
- MYRCIARIA DUBIA FRUIT (UNII: YSW4EM1EKP)
* 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".