FDA.reportPublic FDA data

Ola Botanicals Sunscreen SPF 30

Manufacturer
Natural Health Partners, LLC | Pure Source, LLC
Effective date
2025-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:02:04

Label at a glance#

ProductOla Botanicals Sunscreen SPF 30
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

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

Dosage and administration

apply liberally 15 minutes before sun exposure  children under 6 months of age: Ask a doctor 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 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-sleeve shir...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide (21%)

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn.
  • if used as directed with other sun protection measures (see Directions), sunscreen 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 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

  • apply liberally 15 minutes before sun exposure 
  • children under 6 months of age: Ask a doctor
  • 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 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-sleeve shirts, pants, hats, and sunglasses
  • re-apply:
  • after 40 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Lecithin, Helianthus annuus (Sunflower) Seed OIl, Cetearyl Alcohol, Glycerin, Cetearyl Olivate, Helianthus annuus (Sunflower) Seed Wax, Simmondsia chinensis (Jojoba) Seed Oil, Gluconolactone, Cetearyl Glucoside, Triethoxy-caprylylsilane, Sodium Polyacrylate, Sodium Benzoate, Butyrospermum parkii (Shea) Butter, Cocos nucifera (Coconut) Oil, Xanthan Gum, Eucalyptus globulus Leaf Oil, Calcium Gluconate, Glucose, Aloe barbadensis (Aloe Vera) Leaf Juice, Tocopheryl Acetate, Camellia oleifera Leaf Extract, Punica granatum (Pomegranate) Fruit Extract, Rubus idaeus (Raspberry) Fruit Extract, Citric Acid, Phenoxyethanol, Ethylhexylglycerin.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71239-845-00Ola Botanicals Sunscreen SPF 30236 mL in 1 BOTTLELOTION2361

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71239-84571239-845-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SUNFLOWER OIL3W1JG795YIIACT
CETEARYL ALCOHOL2DMT128M1SIACT
GLYCERINPDC6A3C0OXIACT
CETEARYL OLIVATE58B69Q84JOIACT
HELIANTHUS ANNUUS SEED WAX42DG15CHXVIACT
JOJOBA OIL724GKU717MIACT
GLUCONOLACTONEWQ29KQ9POTIACT
CETEARYL GLUCOSIDE09FUA47KNAIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
SODIUM BENZOATEOJ245FE5EUIACT
SHEA BUTTERK49155WL9YIACT
COCONUT OILQ9L0O73W7LIACT
XANTHAN GUMTTV12P4NEEIACT
EUCALYPTUS OIL2R04ONI662IACT
CALCIUM GLUCONATESQE6VB453KIACT
ANHYDROUS DEXTROSE5SL0G7R0OKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CAMELLIA OLEIFERA LEAF5077EL0C60IACT
POMEGRANATE56687D1Z4DIACT
RASPBERRY4N14V5R27WIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
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
Ola Botanicals Sunscreen SPF 30ZINC OXIDENatural Health Partners, LLCc7a7df0b-da8f-407d-a1ee-28f75070b23c2025-06-02WarningsExact identifier
ndc (package): 71239-845-00
ndc (product): 71239-845
ndc11 (package): 71239084500
spl id: 3694282d-fa57-a94f-e063-6294a90a9ea8
spl set id: c7a7df0b-da8f-407d-a1ee-28f75070b23c

Reported adverse events (FAERS/openFDA)#

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