OTC Medication Information: NYMPHSYN EYE

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.

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

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NYMPHSYN EYE
glycerin cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71276-040
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLYCERIN (GLYCERIN) GLYCERIN 0.29 g in 30 mL
Inactive Ingredients
Ingredient Name Strength
WATER
DICAPRYLYL ETHER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71276-040-02 1 BOTTLE, PUMP in 1 CARTON contains a BOTTLE, PUMP (71276-040-01)
1 NDC:71276-040-01 30 mL in 1 BOTTLE, PUMP This package is contained within the CARTON (71276-040-02)
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 Operations
ULAB 688976692 relabel (71276-040)
Establishment
Name Address ID/FEI Operations
U-LAB Switzerland AG 485958743 manufacture (71276-040)

Revised: 03/2017 ULAB

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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