DAILY LEAVE ON ACNE TREATMENT MASK- benzoyl peroxide cream

Daily Leave on Acne Treatment Mask by

Drug Labeling and Warnings

Daily Leave on Acne Treatment Mask by is a Otc medication manufactured, distributed, or labeled by Allure Labs, Allure LAbs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients
Benzoyl Peroxide 2.5%

PURPOSE

Purpose
Acne Treatment

INDICATIONS & USAGE

Uses
For the treatment of acne

WARNINGS

Warnings
For external use only

DO NOT USE

Do not use
If you have very sensitive skin
Are sensitive to benzoyl
peroxide

WHEN USING

When using this product
Avoid unnecessary sun
exposure & use a sunscreen
Avoid contact with the
eyes, lips, and mouth
Avoid contact with hair &
dyed fabrics, which may
be bleached by this product
Skin irritation may occur,
characterized by redness,
burning, itching, peeling,
or possibly swelling.
Irritation may be reduced
by using the product less
frequently or in a lower
concentration.

STOP USE

Stop use and ask a doctor
If irritation becomes severe

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions
Clean the skin thoroughly
before applying this product
Cover the entire affected
area with a thin layer one
to three times daily
Because excessive drying of
the skin may occur, start with
one application daily, then
gradually increase to two or
three times daily if needed
or as directed by a doctor
If bothersome dryness or
peeling occurs, reduce
application to once a day
or every other day
If going outside, apply
sunscreen after using this
product. If irritation or
sensitivity develops, stop
use of both products and
ask a doctor.

OTHER SAFETY INFORMATION

Other Information
Store at 20°- 25°C (68° - 77°F)

INACTIVE INGREDIENT

Inactive Ingredients
Water (Aqua), Aloe Barbadensis
Leaf Juice, Glycerin, Serenoa
Serrulata (Saw Palmetto) Fruit
Extract, Niacinamide, Linoleic
Acid, Linolenic Acid, Docosahexaenoic
Acid, Eicosapentaenoic
Acid, Scutellaria Baicalensis
Root Extract, Zinc Gluconate,
Tocopherol, Dimethicone,
Silica, Carbomer, Caprylyl
Glycol, Diethylhexyl Sodium
Sulfosuccinate, Ethylhexylglycerin,
Hexylene Glycol, PEG-40
Stearate, Phenoxyethanol,
Propanediol, Sodium
Hydroxide, Sodium Citrate,
Sodium Phytate, Sorbitan
Stearate, Xanthan Gum.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DAILY LEAVE ON ACNE TREATMENT MASK 
benzoyl peroxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4212
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	25 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LINOLENIC ACID (UNII: 0RBV727H71)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
PROPANEDIOL (UNII: 5965N8W85T)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DOCONEXENT (UNII: ZAD9OKH9JC)
SAW PALMETTO (UNII: J7WWH9M8QS)
NIACINAMIDE (UNII: 25X51I8RD4)
ICOSAPENT (UNII: AAN7QOV9EA)
DIMETHICONE (UNII: 92RU3N3Y1O)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PEG-40 STEARATE (UNII: ECU18C66Q7)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
PHYTATE SODIUM (UNII: 88496G1ERL)
XANTHAN GUM (UNII: TTV12P4NEE)
LINOLEIC ACID (UNII: 9KJL21T0QJ)
ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
DOCUSATE SODIUM (UNII: F05Q2T2JA0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4212-2	1 in 1 CARTON	04/02/2022
1	NDC: 62742-4212-1	45 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	04/02/2022

Labeler - Allure Labs (926831603)

Registrant - Allure Labs (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure LAbs		926831603	manufacture(62742-4212)