FDA.reportPublic FDA data

Basic Essentials Acne Wash

Manufacturer
Mission Series Inc. dba Prestige Beauty Care
Effective date
2021-11-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:29:55

Label at a glance#

ProductBasic Essentials Acne Wash
Active ingredientSALICYLIC ACID
Label structure6 sections

Indications and uses

for treatment of acne.

Dosage and administration

Use twice a day. Wet face. Apply to hands, add water and work into a lather. Massage into your face, rinse.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

for treatment of acne.

Warnings

WARNINGS SECTION

For external use only

Ask a doctor if you are using 

OTC - ASK DOCTOR SECTION

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

When using this product

OTC - WHEN USING SECTION

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

Avoid contact with hair, dyed fabric, including carpet and clothing which may be bleached by this product.

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

Use twice a day. Wet face. Apply to hands, add water and work into a lather. Massage into your face, rinse.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium C12-15 Pareth-15 Sulfonate, Aloe Barbadensis Extract, Chamomilla Recutita (Matricaria) Extract, Linoleamidopropyl PG-Dimonium Chloride Phosphate, Disodium Chloride Phosphate, Disodium EDTA, Propylene Glycol, FD&C Yellow 5, FD&C Red 40, Sodium Chloride, Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73597-02373597-023-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM C12-15 PARETH-15 SULFONATE353VA59XH8IACT
MATRICARIA CHAMOMILLA WHOLEG0R4UBI2ZZIACT
LINOLEAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE5Q87K461JOIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C RED NO. 40WZB9127XOAIACT
SODIUM CHLORIDE451W47IQ8XIACT
SALICYLIC ACIDO414PZ4LPZACTIB
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS22ADO53M6FIACT

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
cfcfe223-ecd6-5a6a-e053-2a95a90a3a83cfb8f8f0-a4e4-be2b-e053-2a95a90a0dcd2021-11-02WarningsExact identifier
spl id: cfcfe223-ecd6-5a6a-e053-2a95a90a3a83
spl set id: cfb8f8f0-a4e4-be2b-e053-2a95a90a0dcd

Reported adverse events (FAERS/openFDA)#

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