FDA.reportPublic FDA data

Zapzyt Acne Wash Cleanser

Manufacturer
Denison Pharmaceuticals, LLC
Effective date
2022-11-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:49:11

Label at a glance#

ProductZapzyt Acne Wash Cleanser
Active ingredientSALICYLIC ACID
Label structure8 sections

Dosage and administration

use twice daily apply to hands add water massage gently to the affected area rinse thoroughly

Storage and handling

Store at room temperature 15º-30ºC (59º-86ºF).

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

For the treatment of acne.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, flush thoroughly with water.

using other topical acne medications at the same time or immediately following the 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 physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

For the treatment of acne.

Directions

DOSAGE & ADMINISTRATION SECTION

  • use twice daily
  • apply to hands
  • add water
  • massage gently to the affected area
  • rinse thoroughly

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature 15º-30ºC (59º-86ºF).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Chamomilla Recutita (Matricaria) Flower Extract, Cocamidopropyl Betaine, Disodium EDTA, DMDM Hydantoin, PEG-120 Methyl Glucose Dioleate, Propylene Glycol, Purified Water, Sodium C14-16 Olefin Sulfonate, Sodium Chloride, Sodium Hydroxide

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0295-90550295-9055-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT
SODIUM HYDROXIDE55X04QC32IIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SALICYLIC ACIDO414PZ4LPZACTIB
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
CHAMOMILEFGL3685T2XIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
DMDM HYDANTOINBYR0546TOWIACT
ALOE VERA LEAFZY81Z83H0XIACT
EDETATE DISODIUM7FLD91C86KIACT

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
ecf863df-fc0a-4e28-e053-2a95a90a37ceecf863df-fc14-4e28-e053-2a95a90a37ce2022-11-08WarningsExact identifier
spl id: ecf863df-fc0a-4e28-e053-2a95a90a37ce
spl set id: ecf863df-fc14-4e28-e053-2a95a90a37ce

Reported adverse events (FAERS/openFDA)#

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