NYMPHSYN EYE- glycerin cream 
ULAB

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ACTIVE INGREDIENT

Active ingredients: GLYCERIN 0.97%

INACTIVE INGREDIENT

Inactive ingredients: AQUA (WATER), DICAPRYLYL ETHER, BUTYLENE GLYCOL, STEARIC ACID, GLYCERYL STEARATE, PEG-100 STEARATE, ETHYLHEXYL PALMITATE, PHENOXYETHANOL, CARBOMER, CI 77891 (TITANIUM DIOXIDE), SODIUM POTASSIUM ALUMINUM SILICATE, CETEARYL ALCOHOL, ETHYLHEXYLGLYCERIN, CAFFEINE, POTASSIUM CETYL PHOSPHATE, SODIUM HYDROXIDE, DISODIUM EDTA, MICA, PEG-20 STEARATE, PPG-25-LAURETH-25, SILICA, PEG-8, TRITICUM VULGARE (WHEAT) PROTEIN, PENTYLENE GLYCOL, PALMITOYL DIPEPTIDE-5 DIAMINOBUTYROYL HYDROXYTHREONINE, PALMITOYL DIPEPTIDE-5 DIAMINOHYDROXYBUTYRATE, TOCOPHEROL, SILICA DIMETHYL SILYLATE, ASCORBYL PALMITATE, NICOTIANA SYLVESTRIS LEAF CELL CULTURE, CAPRYLYL GLYCOL, ASCORBIC ACID, CITRIC ACID, SODIUM HYALURONATE, HEXYLENE GLYCOL, SODIUM DEHYDROACETATE, SORBIC ACID, UNDECYLENIC ACID

PURPOSE

Purpose: Restore firmness and tonicity of eye contour area

WARNINGS

Warnings: For external use only Discontinue use if signs of irritation or rashes appear.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

Indications & Usage: Apply morning and night

DOSAGE & ADMINISTRATION

Dosage & Administration: Apply a small amount with fingertips under and around the eye area

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

NYMPHSYN EYE 
glycerin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71276-040
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.29 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DICAPRYLYL ETHER (UNII: 77JZM5516Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71276-040-021 in 1 CARTON03/02/2017
1NDC:71276-040-0130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/02/2017
Labeler - ULAB (688976692)
Registrant - ULAB (688976692)
Establishment
NameAddressID/FEIBusiness Operations
ULAB688976692relabel(71276-040)
Establishment
NameAddressID/FEIBusiness Operations
U-LAB Switzerland AG485958743manufacture(71276-040)

Revised: 3/2017
Document Id: cb5d971b-751f-466d-975e-fddf9126a128
Set id: 4ca5da57-4b8c-481b-b2f5-dbfdfaece471
Version: 1
Effective Time: 20170321
 
ULAB