FDA.reportPublic FDA data

ZINXATION SUNSCREEN LOTION SPF-50

Manufacturer
ANTARIA PTY LTD
Effective date
2020-06-02
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 23:27:26

Label at a glance#

ProductZINXATION SUNSCREEN SPF-50
Active ingredientZINC OXIDE
Label structure8 sections

Indications and uses

Helps prevent sunburn If used as directed with other sun protection measures (see Directions), decreased the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

Apply generously to all areas 20 minutes before sun exposure. Reapply every 2 hours or after swimming.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ZINC OXIDE 25%

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USES

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn
  • If used as directed with other sun protection measures (see Directions), decreased the risk of skin cancer and early skin aging caused by the sun

WARNINGS

WARNINGS SECTION

  • Avoid prolonged exposure in the sun.
  • Wear protective clothing-hats and sunglasses.
  • Do not swallow.
  • For external use only.
  • Avoid contact with eyes.
  • If a rash or irritation occurs discontinue use.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

  • Apply generously to all areas 20 minutes before sun exposure.
  • Reapply every 2 hours or after swimming.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Coco-caprylate/caprate, glycerine, coconut alkane, simmondsia chinensis (jojoba) seed oil, polyglyceryl-3-polyricinoleate, cera alba (beeswax), isostearic acid, polyhydroxy stearic acid, maltodextrin, phenylpropanol, propanediol, caprylyl glycol, tocopherol, ethylhexylglycerin, cetyl phosphate, sodium chloride, disodium EDTA

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

Call +61 73726 2030

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Astiva_ZinXation Face and Body_SPF-50_Page_101b LBL_Astiva_ZinXation Face and Body_SPF-50_Page_1

01b LBL_Astiva_ZinXation Face and Body_SPF-50_Page_201b LBL_Astiva_ZinXation Face and Body_SPF-50_Page_2

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60396-20160396-201-11, 60396-201-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
GLYCERINPDC6A3C0OXIACT
COCONUT ALKANES1E5KJY107TIACT
JOJOBA OIL724GKU717MIACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
YELLOW WAX2ZA36H0S2VIACT
ISOSTEARIC ACIDX33R8U0062IACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
MALTODEXTRIN7CVR7L4A2DIACT
PHENYLPROPANOL0F897O3O4MIACT
PROPANEDIOL5965N8W85TIACT
CAPRYLYL GLYCOL00YIU5438UIACT
TOCOPHEROLR0ZB2556P8IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CETYL PHOSPHATEVT07D6X67OIACT
SODIUM CHLORIDE451W47IQ8XIACT
EDETATE DISODIUM7FLD91C86KIACT
ZINC OXIDESOI2LOH54ZACTIM

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
b4e85227-8c55-521e-e053-2a95a90a81a684dc3c8a-8ab7-4a5c-ab62-beb29aade9ed2020-11-25WarningsExact identifier
spl set id: 84dc3c8a-8ab7-4a5c-ab62-beb29aade9ed

Reported adverse events (FAERS/openFDA)#

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