ACTIVE INGREDIENTS

Manufacturer
ATOMY CO., LTD. | Kolmar Korea Co., Ltd
Effective date
2026-06-02
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-06-06 05:10:17

Label at a glance#

ProductATOMY BB SUNSCREEN
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure8 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

• Apply liberally 15 minutes before sun exposure • Reapply at least every 2 hours • Use a water-resistant sunscreen if swimming or sweating • Children under 6 months: 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 a Broad Spectrum SPF value of 15 or higher and other sun protection measur...

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 8.22%
Zinc Oxide 5.76%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aqua/Water/Eau, Butylene Glycol, Cyclopentasiloxane, Isopropyl Palmitate, Almond Oil, Butylene Glycol Dicaprylate/Dicaprate, Butyloctyl Salicylate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyldecyl Myristoyl Methylaminopropionate, Cyclohexasiloxane, Niacinamide, Talc, Dimethicone/Vinyl Dimethicone Crosspolymer, Dipentaerythrityl Hexahydroxystearate/Hexastearate/Hexarosinate, Hydrogenated Poly(C6-14 Olefin), Magnesium Sulfate, Phytosqualane, Polyglyceryl-4 Isostearate, Purslane Extract, Iron Oxides, Triethoxycaprylylsilane, Disteardimonium Hectorite, Caprylyl Glycol, Glyceryl Caprylate, Trihydroxystearin, Aminopropyl Dimethicone, Polymethylsisesquioxane, Fragrance (Parfum), Alumina, Tea Leaf Extract, Silica Dimethyl Silylate, Tocopheryl Acetate, Silica, Dimethicone, Marshmallow Leaf/Root Extract, Borage Extract, Lemon Balm Leaf Extract, Rosemary Extract

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

WARNINGS

WARNINGS SECTION

For external use only
Do not useon damaged or broken skin
When using this productkeep out of eyes. Rinse with water to remove.
Stop use and ask a doctorif 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.

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

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply liberally 15 minutes before sun exposure
• Reapply at least every 2 hours
• Use a water-resistant sunscreen if swimming or sweating
• Children under 6 months: 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 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton ImageCarton Image

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.atomy.com/bb sunscreen carton.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52257-1430-12024-01-31C16284748780-11030e364-fa55-111a-e063-dadaa90a10e2b0cd27ee-4917-4800-bcdf-c6e14b28c1d1
52257-1430-12024-01-31C16284748780-11030e364-fa55-111a-e063-dadaa90a10e2b0cd27ee-4917-4800-bcdf-c6e14b28c1d1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52257-143052257-1430-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32024-01-31full-release2026-06-01 00:08:10

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
ATOMY BB SUNSCREENTITANIUM DIOXIDE, ZINC OXIDEATOMY CO., LTD.b0cd27ee-4917-4800-bcdf-c6e14b28c1d12026-06-02WarningsExact identifier
ndc (package): 52257-1430-1
ndc (product): 52257-1430
ndc11 (package): 52257143001
spl id: 53421317-2f22-b017-e063-6294a90a41f2
spl set id: b0cd27ee-4917-4800-bcdf-c6e14b28c1d1

Reported adverse events (FAERS/openFDA)#

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