FDA.reportPublic FDA data

Native Mineral Suncare Zinc Oxide Sunscreen Spray Pear and Coconut WaterBroad Spectrum SPF 30

Manufacturer
Twincraft Inc.
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:46:11

Label at a glance#

ProductNative Mineral Suncare Zinc Oxide Sunscreen Pear and Coconut Water Broad Spectrum SPF 30
Active ingredientZINC OXIDE
Label structure10 sections

Indications and uses

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

Dosage and administration

shake well spray liberally and spread evenly by hand 15 minutes before sun exposure hold container 4 to 6 inches from the skin to apply do not spray directly into face. Spray on hands then apply to face reapply at least every 2 hours use water resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk,...

Storage and handling

protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

ZINC OXIDE 20%

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. Rinse with water to remove.
  • keep away from face to avoid breahing it.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help, or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well
  • spray liberally and spread evenly by hand 15 minutes before sun exposure
  • hold container 4 to 6 inches from the skin to apply
  • do not spray directly into face. Spray on hands then apply to face
  • reapply at least every 2 hours
  • use water resistant sunscreen if swimming or sweating
  • 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 sun, especially from 10 a.m. – 2 p.m.
    • wear long-sleeved shirts, pants, hats, and sunglasses
  • children under 6 months: ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • protect this product from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, caprylic/capric triglyceride, coconut alkanes, glycerin, cetearyl alcohol, coco-caprylate/caprate, tocopherol, helianthus annuus (sunflower) seed oil, xanthan gum, coco-glucoside, benzyl alcohol, fragrance, polyhydroxystearic acid

SPL UNCLASSIFIED SECTION

Distr. by Native San Francisco, CA 94111

Questions or comments?

OTC - QUESTIONS SECTION

Please contact support#\@nativecos.com

PRINCIPAL DISPLAY PANEL - 208 mL Bottle, Pump

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30

MINERAL SUNCARE

ZINC OXIDE SUNSCREEN SPRAY

NATIVE

PEAR & COCONUT WATER

BROAD SPECTRUM SPF 30

7 FL OZ (207 mL)

NATNAT

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130030772235690GTIN-13: 0030772235690
EAN-13: 0030772235690
GTIN-12: 030772235690
UPC-A: 030772235690
GTIN storage (14 digits): 00030772235690		NAT.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64412-550764412-5507-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCONUT ALKANES1E5KJY107TIACT
COCO GLUCOSIDEICS790225BIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
TOCOPHEROLR0ZB2556P8IACT
CETEARYL ALCOHOL2DMT128M1SIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
SUNFLOWER OIL3W1JG795YIIACT
BENZYL ALCOHOLLKG8494WBHIACT
XANTHAN GUMTTV12P4NEEIACT
ZINC OXIDESOI2LOH54ZACTIB

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
462d0649-21c5-1856-e063-6294a90ad200462d1f1e-19ed-bd00-e063-6294a90ac74f2025-12-17WarningsExact identifier
spl id: 462d0649-21c5-1856-e063-6294a90ad200
spl set id: 462d1f1e-19ed-bd00-e063-6294a90ac74f

Reported adverse events (FAERS/openFDA)#

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