NYMPHSYN MAXIMIZER- glycerin cream

NYMPHSYN MAXIMIZER by

Drug Labeling and Warnings

NYMPHSYN MAXIMIZER 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 6.29%

INACTIVE INGREDIENT

Inactive ingredients: AQUA (WATER), C12-20 ACID PEG-8 ESTER, CAPRYLIC/CAPRIC TRIGLYCERIDE, BUTYLENE GLYCOL, CYCLOPENTASILOXANE, CETYL ALCOHOL, PHENOXYETHANOL, POTASSIUM CETYL PHOSPHATE DIMETHICONE, CARBOMER, SODIUM POTASSIUM ALUMINUM SILICATE ETHYLHEXYLGLYCERIN, DIMETHICONOL, SODIUM HYDROXIDE, PARFUM (FRAGRANCE), CI 77891 (TITANIUM DIOXIDE), DISODIUM EDTA, MICA, PPG-25-LAURETH-25, SILICA, PALMITOYL TRIPEPTIDE-5, PEG-8, TRITICUM VULGARE (WHEAT) PROTEIN, PENTYLENE GLYCOL, SODIUM HYALURONATE, TOCOPHEROL, ASCORBYL PALMITATE, ASCORBIC ACID, CITRIC ACID, NICOTIANA SYLVESTRIS LEAF CELL CULTURE, SODIUM DEHYDROACETATE, SORBIC ACID, UNDECYLENIC ACID

PURPOSE

Purpose: Moisturizing and lifting for youthful appearance

WARNINGS

Warnings: For external use only Avoid eye contour area 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 morning and night to face and neck after serum and ampoule

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NYMPHSYN MAXIMIZER 
glycerin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71276-060
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	3.14 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
C12-20 ACID PEG-8 ESTER (UNII: 9M7A3K4339)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71276-060-02	1 in 1 CARTON	03/02/2017
1	NDC: 71276-060-01	50 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(71276-060)

Establishment
Name	Address	ID/FEI	Business Operations
U-LAB Switzerland AG		485958743	manufacture(71276-060)