FDA.reportPublic FDA data

do naturals SPF 32

Manufacturer
Dolphin Organics LLC
Effective date
2017-02-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:20:08

Label at a glance#

Productdo naturals SPF 32
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure7 sections

Indications and uses

Helps prevent sunburn. If used as directed withother sun protection measures (see directions),decreases the risk of skin cancer and early skin aging caused by the sun.

Dosage and administration

Apply liberally 15 minutes before sun exposure. Reapply: At least every two-hours. Immediately after swimming, sweating or towel drying. SUN PROTECTION MEASURES: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including: Limit ti...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 6.00%

Zinc Oxide 6.00

Purpose

OTC - PURPOSE SECTION

Sunscreen

USES:

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn.
  • If used as directed withother sun protection measures (see directions),decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS:

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.

Stop use and consult physician

OTC - STOP USE SECTION

if irritation or rash develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical attention or contact poison control center immediately.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sun exposure.
  • Reapply: At least every two-hours. Immediately after swimming, sweating or towel drying.

SUN PROTECTION MEASURES:

  • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including: Limit time in the sun, especially between 10AM and 2PM. Wear long sleeve shirts, pants, hats and sunglasses. For children under 6 months, consult a physician.

OTHER INGREDIENTS:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Avena Sativa (Oat) Betaglucan, Butyrospermum Parkii (Shea) Butter, Camellia Sinensis (Green Tea) Extract, Carthamus Tinctorius (Safflower) Oleosomes, Cetearyl Olivate, Citrullus Lunatus (Watermelon) Extract, Cocos Nucifera (Coconut) Oil, Gluconolactone, Helianthus Annuus (Sunflower) Oil, Mangifera Indica (Mango) Butter, Persea Gratissima (Avocado) Oil, Punica Granatum (Pomegranate) Extract, Simmondsia Chinensis (Jojoba) Oil, Sodium Benzoate, Sorbitan Olivate,
Tocopheryl Acetate (Vitamin E), Xanthan Gum, Zemea (Corn) Propanediol.

Other Information:

SPL UNCLASSIFIED SECTION

*Protect this product from excessive heat and direct sunlight.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130852606003134GTIN-13: 0852606003134
EAN-13: 0852606003134
GTIN-12: 852606003134
UPC-A: 852606003134
GTIN storage (14 digits): 00852606003134		Label.jpg

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70765-75070765-750-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
OATZ6J799EAJKIACT
SHEA BUTTERK49155WL9YIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CARTHAMUS TINCTORIUS SEED OLEOSOMES9S60Q72309IACT
CETEARYL OLIVATE58B69Q84JOIACT
WATERMELON231473QB6RIACT
COCONUT OILQ9L0O73W7LIACT
GLUCONOLACTONEWQ29KQ9POTIACT
HELIANTHUS ANNUUS FLOWERING TOPBKJ0J3D1BPIACT
MANGOI629I3NR86IACT
AVOCADO OIL6VNO72PFC1IACT
PUNICA GRANATUM ROOT BARKCLV24I3T1DIACT
JOJOBA OIL724GKU717MIACT
SODIUM BENZOATEOJ245FE5EUIACT
SORBITAN OLIVATEMDL271E3GRIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
XANTHAN GUMTTV12P4NEEIACT
CORN0N8672707OIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
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
071ba7a3-a26a-7260-e063-6394a90ade092212e3f6-da2c-42b0-99f6-09d4869a6fd52023-10-07WarningsExact identifier
spl set id: 2212e3f6-da2c-42b0-99f6-09d4869a6fd5

Reported adverse events (FAERS/openFDA)#

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