OCEAN BREEZE SCENT

Manufacturer
Zhejiang Gaorong Cosmetic Co., Ltd.
Effective date
2025-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:35:56

Label at a glance#

ProductOCEAN BREEZE SCENT
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Spray product in your palm and rub hands together until dry. For children under 6, use only under adult supervision. Not recommended for infants.

Storage and handling

Do not store above 105°F. May discolor some fabrics. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70%

Purpose

OTC - PURPOSE SECTION

ANTISEPTIC

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease.

When water, soap and towel are not available.

Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.

Stop use and ask a doctor if

OTC - DO NOT USE SECTION

Redness of irritation develop.

Condition persists for more than 72 hours.

When using this product:

OTC - WHEN USING SECTION

Keep out of eyes, ears, or mouth.

In case of eye contact, flush eyes thoroughly with water.

Avoid contact with broken skin.

Do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Redness of irritation develop.

Condition persists for more than 72 hours.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray product in your palm and rub hands together until dry.

For children under 6, use only under adult supervision.

Not recommended for infants.

Others information

STORAGE AND HANDLING SECTION

Do not store above 105°F.

May discolor some fabrics.

Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Dipropylene Glycol, Glycereth-26, Fragrance, Butylene Glycol, Leuconostoc/Radish Root Ferment Filtrate, Aloe Barbadensis Leaf Juice, Phenoxyethanol. May Contain: Red 40 Lake (Cl 16035), Red 33 Lake (CI 17200), Red 4 Lake (CI 14700), Yellow 5 Lake (CI 19140:1), Blue 1 Lake (CI 42090:2)

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children should be supervised by an adult when using this product.

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85472-00385472-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
3abd5210-2fb8-6a8a-e063-6394a90a2ebb39de6df6-e155-aca8-e063-6394a90a7fc12025-07-25WarningsExact identifier
spl set id: 39de6df6-e155-aca8-e063-6394a90a7fc1

Reported adverse events (FAERS/openFDA)#

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