OXY OVERNIGHT ACNE REDUCING PATCHES- salicylic acid patch
The Mentholatum Company

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Drug Facts - OXY Overnight Acne Reducing Patches

Active ingredient

Salicylic acid 0.5%

Purpose

Salicylic acid - Acne treatment

Uses

treats and helps prevent acne

Warnings

For external use only

When using this product

keep away from eyes, lips and mouth. If contact occurs, flush thoroughly with water.
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.

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children.

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

Directions

cleanse skin thoroughly before applying this product
apply patch(es) to affected area(s)
to remove, gently peel back patch and discard
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

Inactive ingredients

acrylates/ethylhexyl acrylate copolymer, water, nonoxynol-30, alcohol denatured, butylene glycol, C13-14 isoparaffin, epilobium angustifolium flower/leaf/stem extract, kaolin, laureth-7, melaleuca alternifolia (tea tree) leaf oil, phenoxyethanol, phytosphingosine, polysorbate 80, PVP, sodium hyaluronate, sodium hydroxide, sodium metabisulfite, sodium polyacrylate, vitis vinifera (grape) seed extract, volcanic ash

Questions?

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

Principal Display Panel

Principal Display Panel

OXY OVERNIGHT ACNE REDUCING PATCHES
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10742-8177
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg

Ingredient Name	Strength
Inactive Ingredients
2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)
WATER (UNII: 059QF0KO0R)
NONOXYNOL-30 (UNII: JJX07DG188)
ALCOHOL (UNII: 3K9958V90M)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
EPILOBIUM ANGUSTIFOLIUM WHOLE (UNII: C278QS9YBT)
KAOLIN (UNII: 24H4NWX5CO)
LAURETH-7 (UNII: Z95S6G8201)
TEA TREE OIL (UNII: VIF565UC2G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
VITIS VINIFERA SEED (UNII: C34U15ICXA)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10742-8177-1	30 in 1 PACKAGE; Type 0: Not a Combination Product	01/01/2018	03/17/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	01/01/2018	03/17/2024

Labeler - The Mentholatum Company (002105757)

Registrant - The Mentholatum Company (002105757)

Name	Address	ID/FEI	Business Operations
Establishment
The Mentholatum Company		002105757	manufacture(10742-8177)

Revised: 11/2025

Document Id: 4402a388-02da-0605-e063-6394a90a8992

Set id: d9652f3f-bb6e-4d74-88d6-d4dbaa3de22d

Version: 9

Effective Time: 20251120

The Mentholatum Company