NYMPHSYN EYE- glycerin cream

NYMPHSYN EYE by

Drug Labeling and Warnings

NYMPHSYN EYE by is a Otc medication manufactured, distributed, or labeled by ULAB, U-LAB Switzerland AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

NYMPHSYN EYE 
glycerin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71276-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.29 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71276-040-02	1 in 1 CARTON	03/02/2017
1	NDC: 71276-040-01	30 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/02/2017

Labeler - ULAB (688976692)

Registrant - ULAB (688976692)

Establishment
Name	Address	ID/FEI	Business Operations
ULAB		688976692	relabel(71276-040)

Establishment
Name	Address	ID/FEI	Business Operations
U-LAB Switzerland AG		485958743	manufacture(71276-040)