OXY OVERNIGHT ACNE REDUCING PATCHES- salicylic acid patch

OXY Overnight Acne Reducing Patches by

Drug Labeling and Warnings

OXY Overnight Acne Reducing Patches by is a Otc medication manufactured, distributed, or labeled by The Mentholatum Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

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

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

Inactive Ingredients
Ingredient Name	Strength
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)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	01/01/2018

Labeler - The Mentholatum Company (002105757)