Label: AUQUEST ADVANCEDRETINOL MOISTURIZING FACIAL CREAM- advancedretinol moisturizing facial cream cream
- NDC Code(s): 84186-014-01
- Packager: Guangzhou Bonnieco Cosmetics Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 9, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
-
Do not use
It's known that with age, skin begins to lose firmness and elasticity. In theupgraded recipe, based on the existing retinol series, revolutionary retinoland niacinamide are merged and then added into Advanced Retinol,Moisturizing Facial Cream to fix multiple skin problems. Retinol is a popularingredient on anti-aging and niacinamide also plays a good role on skinwhitening. Wrinkles, dullness and spots can be all solved in this bottle.
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
- Directions
-
Inactive ingredients
AQUA, SODIUM HYALURONATE,AMMONIUM ACRYLOYLDl-METHYLTAURATE/VP COPOLYMER, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER,TOCOPHETYL ACETATE, HYDROXYPINACOLONE RETINOATE, DIMETHYLISOSORBIDE, 1,2-HEXANEDIOL,PEG/PPG-17/6 COPOLYMER,GLYCERIN CHAMOMILLA RECUTITA(MATRICARIA) FLOWER EXTRACT, TARAXACUM OFFICINALE(DANDELION) RHIZOME/ROOT EXTRACT, CIOLA YEDOENSIS EXTRACT, PAEONIA ALBIFLORA ROOT EXTRACT,MALVA SYLVESTRIS(MALLOW)FLOWER EXTRACT, KlNGINKA EKISU, ALOE BARBADENSIS LEAFJUICE, PHENOXYETHANOL,CERAMIDE NP, CERAMIDE AP, CERAMIDE EOP,PHYTOSPHINGOSINE,CHOLESTEROL, SODIUM LAUROYLLACTYLATE,CARBOMER,XANTHAN GUM,GALACTOMYCESFERMENT FILTRATE,1,2-HEXANEDIOL,ETHYLHEXYLGLYCERIN, ALPHA-ARBURIN,NIACINAMIDE,AROMA, CI 19140, CI 15985,ETHYLHEXYL PALMITATE, DISODIUM EDTA, POLYETHYLEME, PHENOXYETHANOL, CHLORPHENESIN, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER,TRIETHANOLAMINE,CL77492,TRIETHOXYCAPRYLYLSILANE
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
AUQUEST ADVANCEDRETINOL MOISTURIZING FACIAL CREAM
advancedretinol moisturizing facial cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84186-014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 2-BUTYNE-1,4-DIOL (UNII: AXH202FPQM) (2-BUTYNE-1,4-DIOL - UNII:AXH202FPQM) 2-BUTYNE-1,4-DIOL 10 g in 100 g Inactive Ingredients Ingredient Name Strength PTEROPTERIN (UNII: 0YK15S31J3) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLHEXYL PALMITATE (UNII: 2865993309) WATER (UNII: 059QF0KO0R) MALVA SYLVESTRIS FLOWER (UNII: 12X9JI52BS) PHENOXYETHANOL (UNII: HIE492ZZ3T) HYDROXYPINACOLONE RETINOATE (UNII: NJ3V2F02E1) PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CHAMOMILE (UNII: FGL3685T2X) DIHYDROXYISOPROPYL PALMOYLPALMAMIDE (UNII: AQS41C86VI) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) TARAXACUM OFFICINALE (UNII: 39981FM375) NIACINAMIDE (UNII: 25X51I8RD4) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) CERAMIDE NP (UNII: 4370DF050B) CHLORPHENESIN (UNII: I670DAL4SZ) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) CHOLESTEROL (UNII: 97C5T2UQ7J) ALPHA-ARBUTIN (UNII: 72VUP07IT5) HYALURONATE SODIUM (UNII: YSE9PPT4TH) METHYL HEXYL ETHER (UNII: R99K6ANQ7T) LUPINUS KINGII WHOLE (UNII: 2KT5T2V20C) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) ALLANTOIN (UNII: 344S277G0Z) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) CERAMIDE AP (UNII: F1X8L2B00J) GEOTRICHUM CANDIDUM (UNII: 5964J742O8) PEG/PPG-17/6 COPOLYMER (UNII: P5QZM4T259) GLYCERIN (UNII: PDC6A3C0OX) XANTHAN GUM (UNII: TTV12P4NEE) SURFOMER (UNII: 95S6LH9UEV) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84186-014-01 50 g in 1 CANISTER; Type 0: Not a Combination Product 04/09/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/09/2024 Labeler - Guangzhou Bonnieco Cosmetics Co., Ltd (412244189) Establishment Name Address ID/FEI Business Operations Guangzhou Bonnieco Cosmetics Co., Ltd 412244189 label(84186-014) , manufacture(84186-014)