NYMPHSYN FACE MASK- glycerin cream

NYMPHSYN FACE MASK by

Drug Labeling and Warnings

NYMPHSYN FACE MASK 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 2.8%

INACTIVE INGREDIENT

Inactive ingredients: AQUA (WATER), BUTYLENE GLYCOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, COCO-CAPRYLATE/CAPRATE, C12-20 ACID PEG-8 ESTER, POTASSIUM CETYL PHOSPHATE, PHENOXYETHANOL, CI 77891 (TITANIUM DIOXIDE), CARBOMER, POLYACRYLAMIDE, SODIUM POTASSIUM ALUMINUM SILICATE, ETHYLHEXYLGLYCERIN, C13-14 ISOPARAFFIN, CHONDRUS CRISPUS POWDER (CARRAGEENAN), CARAMEL, SODIUM HYDROXIDE, MICA, PARFUM (FRAGRANCE), DISODIUM EDTA, SILICA, LAURETH-7, PEG-8, TRITICUM VULGARE (WHEAT) PROTEIN, PENTYLENE GLYCOL, SODIUM HYALURONATE, TETRADECYL AMINOBUTYROYLVALYLAMINOBUTYRIC UREA TRIFLUOROACETATE TOCOPHEROL, ASCORBYL PALMITATE, MAGNESIUM CHLORIDE, ASCORBIC ACID, CITRIC ACID, NICOTIANA SYLVESTRIS LEAF CELL CULTURE

PURPOSE

Purpose: Skin firming and remodeling

WARNINGS

Warnings: For external use only Avoid contact with eyes. 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: Use one to three times a week

DOSAGE & ADMINISTRATION

Dosage & Administration: - Apply a generous, even layer to clean skin - Leave on for 5 to 10 minutes, then wash-off or leave on over-night

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NYMPHSYN FACE MASK 
glycerin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71276-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1.4 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71276-030-02	1 in 1 CARTON	03/02/2017
1	NDC: 71276-030-01	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(71276-030)

Establishment
Name	Address	ID/FEI	Business Operations
U-LAB Switzerland AG		485958743	manufacture(71276-030)