Sunscreen

Manufacturer
True Botanicals
Effective date
2025-10-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:38:25

Label at a glance#

ProductSunscreen
Active ingredientZINC OXIDE
Label structure9 sections

Indications and uses

- Helps prevent sunburn - If used as directed with other sun protection measures, decreases the risk of sun cancer and early signs of aging caused by the sun

Dosage and administration

- Shake Well. Apply lierally 15 minutes before sun exposure. Layer for additional coverage. - Reapply at least every 2 hours. - Use a water repellant sunscreen if swimming or sweating: immediately after towel drying at least every 2 hours.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 18%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

- Helps prevent sunburn

- If used as directed with other sun protection measures, decreases the risk of sun cancer and early signs of aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

When using product

OTC - WHEN USING SECTION

keep out of eyes.
Rinse with water to remove.

Stop use and ask doctor

OTC - STOP USE SECTION

if rash occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

- Shake Well. Apply lierally 15 minutes before sun exposure. Layer for additional coverage.

- Reapply at least every 2 hours.

- Use a water repellant sunscreen if swimming or sweating: immediately after towel drying at least every 2 hours.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, squalane, polyglyceryl-3
diisostearate, caprylic/capric triglyceride, glyceryl caprylate,
polyhydroxystearic acid, sesamum indicum (sesame) seed
oil, sodium chloride, silybum marianum (milk thistle) ethyl
ester, pisum sativum (pea) peptide, terminalia chebula fruit
extract, rubus idaeus (raspberry) seed oil, niacinamide,
glycerin, sclerotium gum, caprylhydroxamic acid, allantoin,
leuconostoc/radish root ferment filtrate, tocopherol.
May Contain: titanium dioxide, iron oxides

Other information

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun.

Questions or Comments

OTC - QUESTIONS SECTION

Call 1-888-416-0870 M-F 9am-5pm EST

Everyday Skin Tint label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Everyday Skin Tint labelEveryday Skin Tint label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82516-202-01Sunscreen30 g in 1 BOTTLE, PUMPLOTION304
82516-202-02Sunscreen1 in 1 CARTONLOTION14

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82516-20282516-202-01, 82516-202-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ZINC OXIDESOI2LOH54ZACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32024-10-28full-release2026-06-01 00:34:00

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
SunscreenEVERYDAY SKIN TINT SPF 30True Botanicalse17ee943-8f6f-630d-e053-2995a90ae40e2025-10-08WarningsExact identifier
ndc (package): 82516-202-01
ndc (package): 82516-202-02
ndc (product): 82516-202
ndc11 (package): 82516020201
ndc11 (package): 82516020202
spl id: 40a8a749-92b7-d0b4-e063-6294a90ae79f
spl set id: e17ee943-8f6f-630d-e053-2995a90ae40e

Reported adverse events (FAERS/openFDA)#

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