Glossier zit stick breakout eraser

Manufacturer
Glossier Inc.
Effective date
2020-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:24:33

Label at a glance#

ProductGlossier zit stick breakout eraser
Active ingredientBENZOYL PEROXIDE
Label structure10 sections

Indications and uses

• for the treatment/ of acne • penetrates pores to reduce acne breakouts

Dosage and administration

• 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 outs...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzoyl Peroxide 5.0%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

• for the treatment/ of acne
• penetrates pores to reduce acne breakouts

Warnings

WARNINGS SECTION

For external use only
Using other topical acne medications at the same time or immediately following use of this
product may increase dryness or irritation of the skin. If this occurs, only one medication should
be used unless directed by a doctor.

Do not use if you • have very sensitive skin • are sensitive to benzoyl peroxide

When using this product • avoid contact with the eyes, lips, and mouth
• if contact occurs, rinse thoroughly with water • avoid unnecessary sun exposure and
use a sunscreen • avoid contact with hair and 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 and ask a doctor
• if irritation becomes severe

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• 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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Dimethyl Isosorbide, Glycerin, Acrylamide/Sodium
Acryloyldimethyltaurate Copolymer, Propanediol, Niacinamide, Capryloyl Salicylic Acid,
Butylene Glycol, Melaleuca Alternifolia Leaf Oil, Cucumis Sativus (Cucumber) Fruit Extract,
Isohexadecane, Saccharide Isomerate, Xanthan Gum, Polysorbate 80, Polyglyceryl-2
Isostearate, Hydroxyacetophenone, 1,2-Hexanediol, Caprylyl Glycol, Sodium Citrate, Citric Acid,
Ethylhexylglycerin, Disodium EDTA, Diethylhexyl Sodium Sulfosuccinate, Carbomer, Sodium
Hydroxide, Dimethicone, Sorbitan Stearate, PEG-40 Stearate, Phenoxyethanol, Silica, Tocopherol

Other Information

OTHER SAFETY INFORMATION

• store at 20°-25°C (68°-77°F)

Questions or comments?

OTC - QUESTIONS SECTION

visit Glossier.com, email us at gTEAM@glossier.com, or call toll-free 1-844-654-8326

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

71425-040-0371425-040-03

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71425-040-032023-08-27C16284748780-1d6a99b39-a9f1-a426-e053-dadaa90af4c2DRUG FACTS
71425-040-032022-01-28C16284748780-1d6a99b39-a9f1-a426-e053-dadaa90af4c2DRUG FACTS

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71425-04071425-040-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
03e740a5-3727-1e39-e063-6294a90a7128e6ac3d02-f2b3-48cd-89c4-0da01c1ed74a2023-08-27WarningsExact identifier
spl set id: e6ac3d02-f2b3-48cd-89c4-0da01c1ed74a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.