FDA.reportPublic FDA data

Acne Control Clarifying Body Spray

Manufacturer
Murad, LLC | Cosway Company, Inc.
Effective date
2021-07-02
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:41:49

Label at a glance#

ProductAcne Control Clarifying Body Spry
Active ingredientSALICYLIC ACID
Label structure10 sections

Dosage and administration

clean the skin thoroughly before applying product cover the entire affected area with a thin layer one to three times daily because excessive drying of the skin may occur, start with one application daily, then gradually increase to two three 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

Storage and handling

store at room temperature avoid high temperatures protect from freezing keep away from flame, fire and heat

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.5%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Use

INDICATIONS & USAGE SECTION

  • for the management of acne

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the skin thoroughly before applying product
  • cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two three 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

INACTIVE INGREDIENT SECTION

Water (Aqua), Alcohol, Butylene Glycol, PEG-40 Hydrogenated Castor Oil, Niacinamide, Allantoin, Glycerin, Nymphaea Caerulea Flower Extract, Panthenol, Glycolic Acid, Menthol, Tocopheryl Acetate, Sodium Hydroxide, Cocamidopropyl Betaine, t-butyl Alcohol, Citral, Geraniol, Fragrance (Parfum)

Other information

STORAGE AND HANDLING SECTION

  • store at room temperature
  • avoid high temperatures
  • protect from freezing
  • keep away from flame, fire and heat

Questions or comments?

OTC - QUESTIONS SECTION

1.800.33.MURAD or Murad.com

PRINCIPAL DISPLAY PANEL - 130 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

STEP 2
Treat

Murad®

ACNE CONTROL

Clarifying
Body Spray

Treats and helps prevent
body breakouts

0.5% salicylic acid
acne treatment

DEVELOPED BY
+Murad+
EST.
1989
DOCTOR MURAD

e 130mL NET VOL 4.3 FL OZ

PRINCIPAL DISPLAY PANEL - 130 mL Bottle Carton
PRINCIPAL DISPLAY PANEL - 130 mL Bottle Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046487salicylic acid 0.5 % Topical SprayPSN4
1046487salicylic acid 5 MG/ML Topical SpraySCD4
1046487salicylic acid 0.5 % Topical SpraySY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70381-112-022023-01-30C16284748780-1f386c64a-38f3-0266-e053-dadaa90a7c1aAcne Control Clarifying Body Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70381-112-01Acne Control Clarifying Body Spry130 mL in 1 BOTTLESPRAY1304
70381-112-02Acne Control Clarifying Body Spry1 in 1 CARTONSPRAY14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70381-112ACNE CONTROL CLARIFYING BODY SPRY (SALICYLIC ACID) SPRAY [MURAD, LLC]4Legacy NDC, 2 package rows20210808_ff4b1797-6c47-4b39-8a48-218cc8524e1f.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70381-11270381-112-01, 70381-112-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
NIACINAMIDE25X51I8RD4IACT
ALLANTOIN344S277G0ZIACT
GLYCERINPDC6A3C0OXIACT
NYMPHAEA CAERULEA FLOWERS9560USZ74IACT
PANTHENOLWV9CM0O67ZIACT
GLYCOLIC ACID0WT12SX38SIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM HYDROXIDE55X04QC32IIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
TERT-BUTYL ALCOHOLMD83SFE959IACT
CITRALT7EU0O9VPPIACT
GERANIOLL837108USYIACT

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
b9b8e98a-6f13-4593-be2c-7a645dcf910aff4b1797-6c47-4b39-8a48-218cc8524e1f2021-07-02WarningsExact identifier
spl id: b9b8e98a-6f13-4593-be2c-7a645dcf910a
spl set id: ff4b1797-6c47-4b39-8a48-218cc8524e1f

Reported adverse events (FAERS/openFDA)#

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