NYMPHSYN FACE MASK: Package Insert and Label Information

NYMPHSYN FACE MASK- 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 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

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NYMPHSYN FACE MASK
glycerin cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71276-030
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLYCERIN (GLYCERIN) GLYCERIN 1.4 g in 50 mL
Inactive Ingredients
Ingredient Name Strength
WATER
BUTYLENE GLYCOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71276-030-02 1 BOTTLE, PUMP in 1 CARTON contains a BOTTLE, PUMP (71276-030-01)
1 NDC:71276-030-01 50 mL in 1 BOTTLE, PUMP This package is contained within the CARTON (71276-030-02)
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 (71276-030)
Establishment
Name Address ID/FEI Operations
U-LAB Switzerland AG 485958743 manufacture (71276-030)

Revised: 03/2017 ULAB

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