FDA.reportPublic FDA data

Oxy On-The-Go Acne Stick

Manufacturer
The Mentholatum Company
Effective date
2023-04-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:32:59

Label at a glance#

ProductOxy On-The-Go Acne Stick
Active ingredientBENZOYL PEROXIDE
Label structure11 sections

Indications and uses

treats and helps prevent acne

Dosage and administration

clean skin thoroughly before applying this product cover entire affected area with a thin layer 1 to 3 times daily because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 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 ...

Storage and handling

avoid storing at temperatures above 100°F (38°C). THIS PRODUCT MAY BLEACH HAIR OR DYED FABRICS KEEP TIGHTLY CLOSED

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl peroxide 5%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Uses

INDICATIONS & USAGE SECTION

treats and helps prevent acne

Warnings

WARNINGS SECTION

For external use only

Do Not Use if you

OTC - DO NOT USE SECTION

  • have very sensitive skin
  • are sensitive to benzoyl peroxide

When using this product

OTC - WHEN USING SECTION

  • 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 unnecessary sun exposure and use a sunscreen
  • avoid contact with the eyes, lips, and mouth
  • 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 this product less frequently or in a lower concentration.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation becomes severe

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean skin thoroughly before applying this product
  • cover entire affected area with a thin layer 1 to 3 times daily
  • because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 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.
  • Sensitivity Test: Apply product sparingly to a small affected area for the first 3 days. If no discomfort occurs, follow directions above.

Storage and Handling

STORAGE AND HANDLING SECTION

  • avoid storing at temperatures above 100°F (38°C).
  • THIS PRODUCT MAY BLEACH HAIR OR DYED FABRICS
  • KEEP TIGHTLY CLOSED

Inactive Ingredients

INACTIVE INGREDIENT SECTION

dimethicone, methyl methacrylate/glycol dimethacrylate crosspolymer, microcrystalline wax, synthetic wax

Questions

OTC - QUESTIONS SECTION

1-877-636-2677 MON-FRI 9 AM-5 PM (EST)

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Oxy On-The-Go Acne Stick
Oxy On-The-Go Acne Stick

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Facts
Drug Facts

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10742-8304-12023-04-14C16284748780-1f386c649-f5f6-0266-e053-dadaa90a7c1aDrug Facts
10742-8304-12023-01-30C16284748780-1f386c649-f5f6-0266-e053-dadaa90a7c1aDrug Facts

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10742-830410742-8304-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OIACT
METHYL METHACRYLATE196OC77688IACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
SYNTHETIC WAX (1200 MW)Q3Z4BCH099IACT
BENZOYL PEROXIDEW9WZN9A0GMACTIB

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
4402f6cb-eb03-6c64-e063-6294a90a56a445fb31ac-55e5-4401-b416-9e0e83fb4d012025-11-20WarningsExact identifier
spl set id: 45fb31ac-55e5-4401-b416-9e0e83fb4d01

Reported adverse events (FAERS/openFDA)#

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