OTC Purpose

Manufacturer
Overlaps Corp. | CTK OTC Laboratories LLC
Effective date
2026-04-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:54:49

Label at a glance#

ProductOVERLAPS ECTOIN MOIST SUN
Active ingredientOCTISALATE, HOMOSALATE, OCTOCRYLENE, AVOBENZONE
Label structure14 sections

Indications and uses

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

Directions ■ Apply liberally 15 minutes before sun exposure. Reapply at least every two 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 spectrumSPF of 15 or higher and other sun protection measures including: 1) limit time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve sh...

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts
Active Ingredient Purpose
Avobenzone 2.90% ....................................................................Sunscreen
Homosalate 9.00%........................................................................Sunscreen
Octisalate 4.50%.........................................................................Sunscreen
Octocrylene 5.00%........................................................................Sunscreen

OTC Purpose

OTC - PURPOSE SECTION

Purpoise-Sunscreen

Uses

INDICATIONS & USAGE SECTION

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

Do Not Use

OTC - DO NOT USE SECTION

Do Not Use

For external use only
Do not use-on damaged skin, on broken skin

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask Doctor-Stop use and ask a doctor if rash occurs.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

When Using

OTC - WHEN USING SECTION

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

Keep out of reach of children

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

Directions
■ Apply liberally 15 minutes before sun exposure. Reapply at least every two 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 spectrumSPF of 15 or higher and other sun protection measures including: 1) limit time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve shirts, pants, hats, and sunglasses
■ Ask a doctor to use for children under 6 months

Other Information

OTHER SAFETY INFORMATION

Other Information ■ Protect the product in this container from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients
Water, Propanediol, Butyloctyl Salicylate, Dibutyl Adipate, Phenethyl Benzoate, Glycerin, Alcohol Denat., Polymethylsilsesquioxane, Polyglyceryl-3 Distearate, 1,2-Hexanediol, Ectoin, Polyglyceryl-3 Methylglucose Distearate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylyl Glycol, Poly C10-30 Alkyl Acrylate, Tromethamine, Ethylhexylglycerin, Fragrance, Glyceryl Stearate Citrate, Sodium Polyacryloyldimethyl Taurate, Dimethicone, Xanthan Gum, Butylene Glycol, Dimethicone/Vinyl Dimethicone Crosspolymer, Polyglyceryl-10 Myristate, Avena Sativa (Oat) Kernel Extract, Centella Asiatica Extract, Citrus Unshiu Fruit Extract, Houttuynia Cordata Extract, Oryza Sativa (Rice) Bran Extract, Punica Granatum Fruit Extract, Rosa Damascena Flower Extract, Schisandra Chinensis Fruit Extract, Tremella Fuciformis (Mushroom) Extract, Tocopherol, Arginine, Carbomer

Questions or comments?

OTC - QUESTIONS SECTION

​Questions or comments? 1-800-545-8856

Warning

WARNINGS SECTION

For external use only
Do not use ■ on damaged skin
■ on broken skin
Stop use and ask a doctor if rash occurs. When using this product, keep out of eyes. Rinse with water to remove. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel

Overlaps

Ecotin

Moist Sun

Ecotin 0;5%/Rice

Sunscreen Broad Spectrum SPF50

1.69 fl.oz/50 mL

22

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87601-002-01OVERLAPS ECTOIN MOIST SUN50 g in 1 TUBELOTION502
87601-002-02OVERLAPS ECTOIN MOIST SUN20 in 1 BOXLOTION202
87601-002-03OVERLAPS ECTOIN MOIST SUN8 in 1 CARTONLOTION82

Products#

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

DailyMed product names page 1 of 2 · 42 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87601-00287601-002-01, 87601-002-02, 87601-002-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 40 matching rows.

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
OVERLAPS ECTOIN MOIST SUNAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEOverlaps Corp.4c3ed60b-e515-8ff0-e063-6294a90a86df2026-04-22WarningsExact identifier
ndc (package): 87601-002-03
ndc (package): 87601-002-01
ndc (package): 87601-002-02
ndc (product): 87601-002
ndc11 (package): 87601000201
ndc11 (package): 87601000203
ndc11 (package): 87601000202
spl id: 5006ddec-b272-dde7-e063-6294a90a07ec
spl set id: 4c3ed60b-e515-8ff0-e063-6294a90a86df

Reported adverse events (FAERS/openFDA)#

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