FDA.reportPublic FDA data

Daily Hydrating Mineral Body Sunscreen

Manufacturer
Oak Essentials, LLC
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:47:42

Label at a glance#

ProductDaily Hydrating Mineral Body Sunscreen Broad Spectrum SPF 30 Sunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Dosage and administration

apply liberally 15 minutes before sun exposure children under 6 months of age: Ask a doctor use a water-resistant sunscreen if swimming or sweating reapply 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...

Storage and handling

protect the product in this container from excessive heat and direct sun

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 11%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn

Warnings

WARNINGS SECTION

  • For external use only.

OTC - DO NOT USE SECTION

  • Do not use on damaged or broken skin

OTC - WHEN USING SECTION

  • When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

  • Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • children under 6 months of age: Ask a doctor
  • use a water-resistant sunscreen if swimming or sweating
  • reapply 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

Other information

STORAGE AND HANDLING SECTION

  • protect the product in this container from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Caprylic/Capric Triglyceride, Dimethicone, Butylene Glycol, Silica, Cetearyl Alcohol, Cetearyl Olivate, Sorbitan Olivate, Potassium Cetyl Phosphate, Xylitylglucoside, Caprylyl Glycol, Anhydroxylitol, Cetearyl Glucoside, Palmitic Acid, Triethoxycaprylylsilane, Stearic Acid, Xylitol, Glycerin, Pongamia Pinnata Seed Extract, Caprylhydroxamic Acid, Xanthan Gum, Tocopheryl Acetate, Citric Acid, Bioflavonoids, Glycoproteins, Fructooligosaccharides, Pentylene Glycol, Sodium Olivate, Cyamopsis Tetragonoloba (Guar) Gum, Phytic Acid, Fragrance (Parfum).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Oak Essentials SPF - Outer PackagingOak Essentials SPF - Outer PackagingOak Essentials SPF - PDPOak Essentials SPF - PDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87330-101-11Daily Hydrating Mineral Body SunscreenBroad Spectrum SPF 30 Sunscreen178 mL in 1 BOTTLE, PLASTICCREAM1781
87330-101-12Daily Hydrating Mineral Body SunscreenBroad Spectrum SPF 30 Sunscreen50 mL in 1 TUBECREAM501
87330-101-13Daily Hydrating Mineral Body SunscreenBroad Spectrum SPF 30 Sunscreen1 in 1 BOXCREAM11

Products#

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

DailyMed product names page 1 of 1 · 38 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87330-10187330-101-11, 87330-101-12, 87330-101-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETEARYL GLUCOSIDE09FUA47KNAIACT
STEARIC ACID4ELV7Z65APIACT
PONGAMIA PINNATA WHOLE11R319D14OIACT
LITHOPS PSEUDOTRUNCATELLA CULTURED GLYCOCALYX LYSATEEW63SRN2WNIACT
CETEARYL OLIVATE58B69Q84JOIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
BENZYL SALICYLATEWAO5MNK9TUIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PALMITIC ACID2V16EO95H1IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
GLYCERINPDC6A3C0OXIACT
CITRUS BIOFLAVONOIDSBD70459I50IACT
LEMON OIL, COLD PRESSEDI9GRO824LLIACT
CETEARYL ALCOHOL2DMT128M1SIACT
XYLITYLGLUCOSIDEO0IEZ166FBIACT
DIMETHICONE92RU3N3Y1OIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LINALOOL, (+/-)-D81QY6I88EIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
SORBITAN OLIVATEMDL271E3GRIACT
PENTYLENE GLYCOL50C1307PZGIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
CARYOPHYLLENEBHW853AU9HIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM OLIVATEND5Y5M6ZUTIACT
CITRIC ACID2968PHW8QPIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
LONGIFOLENE3YXH7YY8WMIACT
LIME OIL, DISTILLED7937R189CBIACT
XYLITOLVCQ006KQ1EIACT
XANTHAN GUMTTV12P4NEEIACT
CYAMOPSIS TETRAGONOLOBA (GUAR) GUME89I1637KEIACT
ANHYDROXYLITOL8XWR7NN42FIACT
PHYTIC ACID7IGF0S7R8IIACT

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
Daily Hydrating Mineral Body Sunscreen Broad Spectrum SPF 30 SunscreenZINC OXIDEOak Essentials, LLC47d37f44-10b2-214f-e063-6294a90a5abc2026-01-07WarningsExact identifier
ndc (package): 87330-101-12
ndc (package): 87330-101-13
ndc (package): 87330-101-11
ndc (product): 87330-101
ndc11 (package): 87330010112
ndc11 (package): 87330010113
ndc11 (package): 87330010111
spl id: 47d3da7c-c989-3f35-e063-6394a90a86b9
spl set id: 47d37f44-10b2-214f-e063-6294a90a5abc

Reported adverse events (FAERS/openFDA)#

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