NYMPHSYN INTENSIVE SERUM- 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.

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ACTIVE INGREDIENT

Active ingredients: GLYCERIN 6.59%

INACTIVE INGREDIENT

Inactive ingredients: AQUA (WATER), BUTYLENE GLYCOL, POLYMETHYLSILSESQUIOXANE, PENTYLENE GLYCOL, SODIUM POTASSIUM ALUMINUM SILICATE, ALCOHOL DENAT, CAPRYLIC/CAPRIC TRIGLYCERIDE, PEG-8, PHENOXYETHANOL, CYCLOPENTASILOXANE, CI 77891 (TITANIUM DIOXIDE), SILICA, ETHYLHEXYLGLYCERIN, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, DIMETHICONOL, XANTHAN GUM HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, DISODIUM EDTA, PARFUM (FRAGRANCE), LIMNANTHES ALBA (MEADOWFOAM) SEED OIL, SQUALANE, MICA, SODIUM HYDROXIDE, CHONDRUS CRISPUS POWDER (CARRAGEENAN), SODIUM HYALURONATE, POLYSORBATE 60, DIPEPTIDE DIAMINOBUTYROYL BENZYLAMIDE DIACETATE, TRITICUM VULGARE (WHEAT) PROTEIN, BUTYROSPERMUM PARKII (SHEA) BUTTER EXTRACT, SORBITAN ISOSTEARATE, NICOTIANA SYLVESTRIS LEAF CELL CULTURE

PURPOSE

Purpose: Youth aid serum for an immediate and intensive care

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: Apply morning and night

DOSAGE & ADMINISTRATION

Dosage & Administration: Apply morning and night on clean face and neck prior to ampoule and moisturizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

NYMPHSYN INTENSIVE SERUM 
glycerin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71276-050
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN1.97 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71276-050-021 in 1 CARTON03/02/2017
1NDC:71276-050-0130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/02/2017
Labeler - ULAB (688976692)
Registrant - ULAB (688976692)
Establishment
NameAddressID/FEIBusiness Operations
ULAB688976692relabel(71276-050)
Establishment
NameAddressID/FEIBusiness Operations
U-LAB Switzerland AG485958743manufacture(71276-050)

Revised: 3/2017
Document Id: d498810f-39f2-4b88-9b00-80c7df2d8e0e
Set id: be3c7b7d-3eb2-480c-a0b1-543de28dfa30
Version: 1
Effective Time: 20170321
 
ULAB