FDA.reportPublic FDA data

ZINC FIVE-O ZINXATION BABY MINERAL SUNSCREEN

Manufacturer
ANTARIA PTY LTD
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:27:27

Label at a glance#

ProductZINC FIVE-O ZINXATION BABY MINERAL SUNSCREEN SPF-50
Active ingredientZINC OXIDE
Label structure9 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 LIBERALLY AND EVENLY 20 MINUTES BEFORE SUN EXPOSURE REAPPLY:    AFTER 40 MINUTES OF SWIMMING OR SWEATING    IMMEDIATELY AFTER TOWEL DRYING    AT LEAST EVERY 2 HOURS SUN PROTECTION MEASURES: SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THIS RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF VALUE OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDIN...

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

FOR EXTERNAL USE ONLY.

DO NOT USE ON DAMAGED OR BROKEN SKIN.

WHEN USING THIS PRODUCT KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE.

STOP USE AND ASK A DOCTOR IF RASH OCCURS.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

  • APPLY LIBERALLY AND EVENLY 20 MINUTES BEFORE SUN EXPOSURE
  • REAPPLY:
  •    AFTER 40 MINUTES OF SWIMMING OR SWEATING
  •    IMMEDIATELY AFTER TOWEL DRYING
  •    AT LEAST EVERY 2 HOURS
  • SUN PROTECTION MEASURES: SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THIS RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF VALUE OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING:
  •    LIMIT TIME IN THE SUN, ESPECIALLY FROM 10 A.M. - 2 P.M.
  •    WEAR LONG-SLEEVED SHIRTS, PANTS, HATS, AND SUNGLASSES
  • CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR

OTHER INFORMATION

OTHER SAFETY INFORMATION

STORE AT TEMPERATURES BELOW 90°F (30°C). PROTECT THE PRODUCT IN THIS CONTAINER FROM EXCESSIVE HEAT AND DIRECT SUN.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

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

QUESTIONS?

OTC - QUESTIONS SECTION

contactbaby@zincfive0.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_ZINC FIVE-0 BABY FDA_front01b LBL_ZINC FIVE-0 BABY FDA_front

01b LBL_ZINC FIVE-0 BABY FDA_back01b LBL_ZINC FIVE-0 BABY FDA_back

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60396-20960396-209-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
GLYCERINPDC6A3C0OXIACT
COCONUT ALKANES1E5KJY107TIACT
JOJOBA OIL724GKU717MIACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
YELLOW WAX2ZA36H0S2VIACT
ISOSTEARIC ACIDX33R8U0062IACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
MALTODEXTRIN7CVR7L4A2DIACT
ALOE VERA LEAFZY81Z83H0XIACT
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
b33d14e4-cb65-83f1-e053-2a95a90a1262a0a4deb8-a484-421a-ab42-2e28d075c3fd2020-11-03WarningsExact identifier
spl set id: a0a4deb8-a484-421a-ab42-2e28d075c3fd

Reported adverse events (FAERS/openFDA)#

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