FDA Label for Ocean Breeze Scent
View Indications, Usage & Precautions
Ocean Breeze Scent Product Label
The following document was submitted to the FDA by the labeler of this product Zhejiang Gaorong Cosmetic Co., Ltd.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
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.
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.
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.
Package Label.Principal Display Panel
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