By the Beach Suncare

Manufacturer
By the Beach Suncare LLC
Effective date
2025-11-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:16:19

Label at a glance#

ProductBy the Beach Suncare
Active ingredientOCTOCRYLENE
Label structure9 sections

Dosage and administration

Shake well. Apply liberally and evenly 15–20 minutes before sun exposure. Apply to all skin exposed to the sun. Children under 6 months of age: Ask a doctor. Re-apply immediately after spending time in the water. Re-apply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating. Warning: Reducing this quantity will lower the level of protection significantly.

Storage and handling

Protect the product in this container from excessive heat or direct sun. This product helps with UVA & UVB protection.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Octocrylene (10%) – Sunscreen

Octisalate (5%) – Sunscreen

Avobenzone (3%) – Sunscreen

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

Helps prevent sunburn

If used with other sun protection measures (see below), helps decrease the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

Skin Cancer / Skin Aging Alert: Spending time in the sun increases your risk of skin cancer & early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

Over-exposure to the sun is a serious health threat.

Do not use on damaged and/or broken skin.

When using this product keep out of eyes. Rinse with water to remove. External use only.

Stop use and ask a doctor if rash occurs.

Keep infants out of direct sunlight.

Do not stay too long in the sun, even while using a sunscreen product.

Re-apply frequently to maintain protection, especially after perspiring, swimming or toweling.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childeren. Contact a Poison Control Center: This is the emergency contact for accidental overdose or ingestion

Directions

DOSAGE & ADMINISTRATION SECTION

Shake well. Apply liberally and evenly 15–20 minutes before sun exposure.

Apply to all skin exposed to the sun.

Children under 6 months of age: Ask a doctor.

Re-apply immediately after spending time in the water.

Re-apply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating.

Warning: Reducing this quantity will lower the level of protection significantly.

Other information

STORAGE AND HANDLING SECTION

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

This product helps with UVA & UVB protection.

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, OCTOCRYLENE, ETHYLHEXYL SALICYLATE (OCTISALATE), PROPYLENE GLYCOL, ETHYLHEXYL PALMITATE, BUTYL METHOXYDIBENZOYLMETHANE (AVOBENZONE), GLYCERYL STEARATE, PEG-100 STEARATE, LITHIUM MAGNESIUM SILICATE, ELAEIS GUINEENSIS (PALM) OIL, PHENOXYETHANOL, STEARYL ALCOHOL, POLYACRYLAMIDE, FRAGRANCE, POTASSIUM CETYL PHOSPHATE, C13-14 ISOPARAFFIN, XANTHAN GUM, DIMETHICONE, CETYL ALCOHOL, LAURETH-7, ELAEIS GUINEENSIS (PALM) KERNEL OIL, ETHYLHEXYLGLYCERIN, HYDROXYETHYLCELLULOSE, DIMETHICONOL, CI 19140, SODIUM CHLORIDE, DISODIUM PHOSPHATE, POLYSORBATE 60, CI 42090, SODIUM PHOSPHATE

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850035746110GTIN-13: 0850035746110
EAN-13: 0850035746110
GTIN-12: 850035746110
UPC-A: 850035746110
GTIN storage (14 digits): 00850035746110
Melon Label.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87094-112-11By the Beach Suncare118 mL in 1 TUBECREAM1181
87094-112-12By the Beach Suncare177 mL in 1 TUBECREAM1771

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87094-11287094-112-11, 87094-112-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
By the Beach SuncareSPF 30 SUNCARE MALON DAZEBy the Beach Suncare LLC4391728b-dfe7-3ffb-e063-6394a90a240e2025-11-14WarningsExact identifier
ndc (package): 87094-112-12
ndc (package): 87094-112-11
ndc (product): 87094-112
ndc11 (package): 87094011211
ndc11 (package): 87094011212
spl id: 43917be4-d4de-65ac-e063-6294a90aab8a
spl set id: 4391728b-dfe7-3ffb-e063-6394a90a240e

Reported adverse events (FAERS/openFDA)#

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