Label: DR.NUELL WATER FULL SKIN BARRIER LOSESNCE- glycerin, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 73430-0006-1 - Packager: Apharm Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 3, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
1) if there is any abnormal symptom or side effect, such as red spot, swelling and itching when using cosmetlcs or after using due to direct sunlight, consult dermatologists
2) Do not use for wounded areas
3) Precautions for storage and handling
keep out of reach of children, store away from direct sunlight
4) avoid the eye area -
INACTIVE INGREDIENT
SEA WATER
PANTHENOL
BUTYLENE GLYCOL
PENTYLENE GLYCOL
NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE
C12-15 ALKYL BENZOATE
SANGUISORBA OFFICINALIS ROOT EXTRACT
HYDROLYZED COLLAGEN
CENTELLA ASIATICA EXTRACT
ACETYL HEXAPEPTIDE-8
ALLANTOIN
SODIUM HYALURONATE
CERAMIDE 3
HYDROGENATED LECITHIN
MADECASSOSIDE
CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT
GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT
CINNAMOMUM CASSIA BARK EXTRACT
ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT
GLYCINE SOJA (SOYBEAN) SPROUT EXTRACT
PLANKTON EXTRACT
C14-22 ALCOHOLS
1,2-HEXANEDIOL
CETYL ETHYLHEXANOATE
GLYCERYL STEARATE SE
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
C12-20 ALKYL GLUCOSIDE
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL
CAPRYLYL GLYCOL
CAPRYLIC/CAPRIC TRIGLYCERIDE
WATER
CITRUS PARADISI (GRAPEFRUIT) PEEL OIL
LITSEA CUBEBA FRUIT OIL
PELARGONIUM GRAVEOLENS FLOWER OIL
SALVIA OFFICINALIS (SAGE) OIL
DISODIUM EDTA - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.NUELL WATER FULL SKIN BARRIER LOSESNCE
glycerin, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73430-0006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 0.59095 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73430-0006-1 150 mL in 1 PACKAGE; Type 0: Not a Combination Product 11/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part347 11/01/2019 Labeler - Apharm Co., Ltd. (689054266) Registrant - Apharm Co., Ltd. (689054266) Establishment Name Address ID/FEI Business Operations APHARM Co., Ltd. 689054266 manufacture(73430-0006)
