LUSHMAN BLOSSOM REFRESH GREAT PASSION MIST- alcohol liquid

Lushman Blossom Refresh Great Passion Mist by

Drug Labeling and Warnings

Lushman Blossom Refresh Great Passion Mist by is a Otc medication manufactured, distributed, or labeled by BIO-FD&C. Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

Antiseptic

Alcohol

Water, Porphyra 334, Porphyra Yezoensis Extract, Sophora Flavescens Extract, Rosa Damascena Callus Culture Extract, Glycine Max (Soybean) Phytoplacenta Extract, Lavandula Angustifolia (Lavender) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Monarda Didyma Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Freesia Refracta Extract, Butylene Glycol, Limonene, 1,2 Hexanediol, Linalool, Geraniol, Fragrance

For the external use only

. Flammable. Keep away from fire or flame.
For external use only.
When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears
and lasts.
Keep Out of Reach of Children.
Do not eat.
If swallowed, get medical help or contact a Poison Control
Center right away

Directions
Put enough product in your palm to cover hands and rub
hands together briskly until dry.
Children under 6 years of age should be supervised when
using. Not recommended for infants.

Keep out of reach of children

INGREDIENTS AND APPEARANCE

LUSHMAN BLOSSOM REFRESH GREAT PASSION MIST 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76882-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GERANIOL (UNII: L837108USY)
WATER (UNII: 059QF0KO0R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76882-0003-1	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - BIO-FD&C. Co., Ltd. (688203268)

Registrant - BIO-FD&C. Co., Ltd. (688203268)

Establishment
Name	Address	ID/FEI	Business Operations
BIO-FD&C. Co., Ltd.		688203268	manufacture(76882-0003)