DR.ALTHEA WATER GLOW AQUA

Manufacturer
Dr. Althea
Effective date
2016-08-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:46:47

Label at a glance#

ProductDR.ALTHEA WATER GLOW AQUA
Active ingredientPROPOLIS WAX
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

PROPOLIS EXTRACT

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

helps hydrate skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

After washing face in the morning and evening, apply at the last step of skin care

WARNINGS SECTION

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 SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70905-0001-12020-01-31C16284748780-19d75b9d0-205f-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70905-0001-1DR.ALTHEA WATER GLOW AQUA50 mL in 1 JARCREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70905-0001DR.ALTHEA WATER GLOW AQUA (PROPOLIS WAX) CREAM [DR. ALTHEA]2Legacy NDC, 1 package rows20160812_b7a7b4dd-dc92-4024-8015-355ed8c00ebd.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70905-000170905-0001-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PROPOLIS WAX6Y8XYV2NOFACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
39d7a5d2-678d-4c08-e054-00144ff8d46cb7a7b4dd-dc92-4024-8015-355ed8c00ebd2016-08-12WarningsExact identifier
spl id: 39d7a5d2-678d-4c08-e054-00144ff8d46c
spl set id: b7a7b4dd-dc92-4024-8015-355ed8c00ebd

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.