Biore Anti-Blemish In-Shower Flash Treatment

what it does

BIORE ANTI-BLEMISH IN-SHOWER FLASH TREATMENT warms on contact and melts away acne-causing dirt and oil and helps control unwanted breakouts - right in the shower!

Perfect for daily, in-shower use to treat & help prevent acne for oh-so clear skin. #tada

Drug Facts

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Use

clears up acne blemishes and blackheads

Warnings

For external use only.

skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet face
squeeze product into dry hands
massage over entire face
rinse thoroughly

Other information

store at room temperature

Inactive ingredients

Zeolite, PEG-8, Butylene, Glycol, Ethoxydiglycol, Cellulose, Sodium Lauroyl Lactylate, Helianthus Annuus (Sunflower) Seed Wax, Cetearyl Alcohol, Hydroxypropylcellulose, Ceteth-20 Phosphate, Cetyl Dimehticone, Dicetyl Phosphate, Fragrance, BHT, Blue 1 Lake

Questions?

1-888-BIORE-11

www.biore.com

@bioreus

BIORE is a trademark of Kao Corp.

Distributed by Kao USA Inc.

Made in USA of US and Imported Ingredients

Biore

free your pores!

opens pores and targets blemishes

15 SECOND WARMING FACIAL

ANTI-BLEMISH IN-SHOWER FLASH TREATMENT

SALICYLIC ACID ACNE TREATMENT

oil-free

acne's outta here!

NET WT 4.5 OZ (127 g)

10596-191-45-NEW

BIORE ANTI BLEMISH FLASH TREATMENT
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10596-191
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
CETETH-20 PHOSPHATE (UNII: 921FTA1500)
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
ALUMINUM SILICATE (UNII: T1FAD4SS2M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10596-191-45	127 g in 1 TUBE; Type 0: Not a Combination Product	10/01/2019	06/30/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	10/01/2019	06/30/2024

Labeler - Kao USA Inc. (004251617)