Label: DR.ALTHEA WATER GLOW AQUA- propolis wax cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70905-0001-1 - Packager: Dr. Althea
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated August 12, 2016
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
WATER, CYCLOPENTASILOXANE, GLYCERIN, ALCOHOL, BETAINE, PEG-32, HYDROGENATED POLY(C6-14 OLEFIN), HYDROGENATED POLYDECENE, XANTHAN GUM, POLYACRYLAMIDE, 1,2-HEXANEDIOL, DIMETHICONOL, HYDROGENATED LECITHIN, PHENOXYETHANOL, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, C13-14 ISOPARAFFIN, BUTYLENE GLYCOL, TROMETHAMINE, PORTULACA OLERACEA EXTRACT, PUERARIA THUNBERGIANA ROOT EXTRACT, CNIDIUM OFFICINALE ROOT EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, PAEONIA LACTIFLORA ROOT EXTRACT, ACHILLEA MILLEFOLIUM EXTRACT, ALCHEMILLA VULGARIS EXTRACT, AMARANTHUS CAUDATUS SEED EXTRACT, MALVA SYLVESTRIS (MALLOW) EXTRACT, MELISSA OFFICINALIS LEAF, MENTHA PIPERITA (PEPPERMINT) LEAF EXTRACT, PRIMULA VERIS EXTRACT, ULMUS DAVIDIANA ROOT EXTRACT, VERONICA OFFICINALIS FLOWER/LEAF/STEM EXTRACT, LAURETH-7, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, CARBOMER, ETHYLHEXYLGLYCERIN, SOLUBLE COLLAGEN, CITRUS AURANTIUM DULCIS (ORANGE) OIL, DISODIUM EDTA, CITRUS LIMON (LEMON) FRUIT OIL, ALOE BARBADENSIS LEAF JUICE, SODIUM HYALURONATE, CITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL, CYMBOPOGON SCHOENANTHUS OIL, DIMETHICONE, HYDROGENATED POLYISOBUTENE, SQUALANE, CYMBOPOGON NARDUS (CITRONELLA) OIL, GERANIUM MACULATUM OIL, ARGANIA SPINOSA KERNEL OIL, ISONONYL ISONONANOATE, POLYGLYCERYL-10 STEARATE, BUTYROSPERMUM PARKII (SHEA) BUTTER, CETEARYL ALCOHOL, POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, STEARIC ACID SURFACTANT, INULIN LAURYL CARBAMATE, DISODIUM STEAROYL GLUTAMATE
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
1) Occurrence of red spots, swelling, itchiness, and other skin irritation
2) If the symptoms above occur after the application area is exposed to direct sunlight
2. Do not use on open wounds, eczema, and other skin irritations
3. Precaution for Storage and Handling
1) Close the lid after use
2) Keep out of reach of infants and children
3) Do not to store in a place with high/low temperature and exposed to direct sunlight - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.ALTHEA WATER GLOW AQUA
propolis wax creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70905-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROPOLIS WAX (UNII: 6Y8XYV2NOF) (PROPOLIS WAX - UNII:6Y8XYV2NOF) PROPOLIS WAX 0.1 g in 100 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:70905-0001-1 50 mL in 1 JAR; Type 0: Not a Combination Product 08/11/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/11/2016 Labeler - Dr. Althea (689694436) Registrant - Dr. Althea (689694436) Establishment Name Address ID/FEI Business Operations Dr. Althea 689694436 manufacture(70905-0001)
