OCEAN BREEZE SCENT by Zhejiang Gaorong Cosmetic Co., Ltd.

OCEAN BREEZE SCENT by

Drug Labeling and Warnings

OCEAN BREEZE SCENT by is a Otc medication manufactured, distributed, or labeled by Zhejiang Gaorong Cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

OCEAN BREEZE SCENT- alcohol solution 
Zhejiang Gaorong Cosmetic Co., Ltd.

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ETHYL ALCOHOL 70%

Purpose

ANTISEPTIC

Use

To decrease bacteria on the skin that could cause disease.

When water, soap and towel are not available.

Recommended for repeated use.

Warnings

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

Stop use and ask a doctor if

Redness of irritation develop.

Condition persists for more than 72 hours.

When using this product:

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

Redness of irritation develop.

Condition persists for more than 72 hours.

Directions

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

Do not store above 105°F.

May discolor some fabrics.

Harmful to wood finishes and plastics.

Inactive ingredients

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

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

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

OCEAN BREEZE SCENT 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85472-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
WATER (UNII: 059QF0KO0R)
GLYCERETH-26 (UNII: NNE56F2N14)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85472-003-01	35 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/14/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	07/14/2025	07/25/2025

Labeler - Zhejiang Gaorong Cosmetic Co., Ltd. (421318550)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Gaorong Cosmetic Co., Ltd.		421318550	manufacture(85472-003)

Revised: 7/2025

Document Id: 3abd5210-2fb8-6a8a-e063-6394a90a2ebb

34390-5

Set id: 39de6df6-e155-aca8-e063-6394a90a7fc1

Version: 2

Effective Time: 20250725