FDA.reportPublic FDA data

Charmzone ALBATROSS Powder Sun (SPF41 PA)

Manufacturer
CHARMZONE CO LTD
Effective date
2009-11-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:22:51

Label at a glance#

ProductCharmzone ALBATROSS Powder Sun (SPF41 PA)
Active ingredientOCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Label1

WARNINGS:

For external use only.  Avoid contact with eyes.  Keep out of children's reach.

OTC - ACTIVE INGREDIENT SECTION


Label2

INGREDIENTS:

WATER, ETHYLHEXYL METHOXYCINNAMATE, BUTYLENE GLYCOL, POLYMETHYL METHACRYLATE, ETHYLHEXYL DIMETHYL PABA, ETHYLHEXYL SALICYLATE, HYDROGENATED POLYDECENE, ZINC OXIDE, SILICA, CYCLOMETHICONE, BUTYL METHOXYDIBENZOYLMETHANE, BIOSACCHARIDE GUM-1, TITANIUM DIOXIDE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, CETYL ALCOHOL, CETEARETH-12, GLYCERYL STEARATE, PEG-100 STEARATE, SODIUM HYALURONATE, STEARIC ACID, DIETHOXYETHYL SUCCINATE, GLYCERYL POLYACRYLATE, SORBITAN OLIVATE, BEESWAX, CETEARYL OLIVATE, CETYL PALMITATE, AMMONIUM ACRYLOYLDIMETHYLTAURATE / VP COPOLYMER, PHENOXYETHANOL, SORBITAN PALMITATE, TOCOPHERYL ACETATE, POTASSIUM CETYL PHOSPHATE, METHYLPARABEN, TRIETHOXYCAPRYLYLSILANE, FRAGRANCE, BIFIDA FERMENT LYSATE, BUTYLPARABEN, DIPOTASSIUM GLYCYRRHIZATE, HYDROLYZED SOY PROTEIN, MORUS ALBA ROOT EXTRACT, PEG-1182 METHYL ESTER SERICIN, PROPYLPARABEN, XANTHAN GUM, MAGNESIUM ASCORBYL PHOSPHATE, BHT, DIMETHICON, FOMES OFFICINALIS (MUSHROOM) EXTRACT, DISODIUM EDTA, STEARYL GLYCYRRHETINATE, GLYCOSAMINOGLYCANS, ATELOCOLLAGEN, BAMBUSA  ARUNDINACEA STEM EXTRACT, RUBUS SUAVISSIMUS (RASPBERRY) LEAF EXTRACT, PORTULACA OLEACEA EXTRACT, ANGELICA POLYMORPHA SINENSIS ROOT EXTRACT, ASPALATHUS LINEARIS LEAF EXTRACT, VISCUM ALBUM (MISTLETOE) LEAF EXTRACT

OTC - WHEN USING SECTION


Label3

[How to Use]

1) Before outdoor leisure activities, evenly smooth over face (avoid around the eyes), arms, neck, legs and other areas that might be exposed to sunlight.

2) It can be used as under-makeup and helps the color makeup adhere to skin and stay on.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


Label4


LABELLABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
22201-2001-12019-10-21C16284748780-1956f9ecf-bded-621f-e053-dbdaa90a74ad7716c299-e286-4a19-83ad-fac91a908b47

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
22201-2001-1Charmzone ALBATROSS Powder Sun (SPF41 PA)70 mL in 1 TUBECREAM701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
22201-2001CHARMZONE ALBATROSS POWDER SUN (SPF41 PA) (OCTINOXATE OCTISALATE ZINC OXIDE TITANIUM DIOXIDE) CREAM [CHARMZONE CO LTD]1Legacy NDC, 1 package rows20091201_7716c299-e286-4a19-83ad-fac91a908b47.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
TITANIUMACTIVE MOIETYD1JT611TNE1
ZINCACTIVE MOIETYJ41CSQ7QDS1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
22201-200122201-2001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB

Source Document#

Source XML

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
5d7f20ed-e64b-4c80-8695-e27eeaa0c5337716c299-e286-4a19-83ad-fac91a908b472009-11-09Exact identifier
spl id: 5d7f20ed-e64b-4c80-8695-e27eeaa0c533
spl set id: 7716c299-e286-4a19-83ad-fac91a908b47

Reported adverse events (FAERS/openFDA)#

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