FDA.reportPublic FDA data

Rapid Action Daily Face Wash

Manufacturer
Rite Aid | Product Quest Mfg
Effective date
2018-06-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:49

Label at a glance#

ProductRapid Action Daily Face Wash Daylogic
Active ingredientSalicylic Acid
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                        Purpose
Salicylic Acid 2%.........................................Acne Treatment

INDICATIONS & USAGE SECTION

Use For the treatment of acne.

WarningsFor external use only.

WARNINGS SECTION

When using this product • skin irritation and dryness are 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 swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions • Cleanse twice a day. • Wet face. Apply to hands, add water and work into a lather. • Massage face gently. • Rinse thoroughly.

INACTIVE INGREDIENT SECTION

Inactive ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer
Cetearyl Alcohol
Cistus Monspeliensis Extract
Disodium EDTA
Fragrance
Glycerin
Helichrysum Italicum Extract
Lavandula Stoechas Extract
Sodium Cocamidopropyl Betaine
Sodium Cocoyl Isethionate
Sodium Hydroxide
Sodium Laureth Sulfate
Waters

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
562600salicylic acid 2 % Medicated Liquid SoapPSN1
562600salicylic acid 20 MG/ML Medicated Liquid SoapSCD1
562600salicylic acid 2 % Facial Cleanser TonerSY1
562600salicylic acid 2 % Facial ScrubSY1
562600salicylic acid 2 % Medicated Liquid SoapSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-7802-52020-01-31C16284748780-19d75b9cf-cf4d-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-7802-5Rapid Action Daily Face WashDaylogic201 mL in 1 TUBECREAM2011

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-7802RAPID ACTION DAILY FACE WASH DAYLOGIC (SALICYLIC ACID) CREAM [RITE AID]1Legacy NDC, 1 package rows20180607_d0f820f7-bd6d-4a18-a9c4-7f0293259bcf.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-780211822-7802-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
Salicylic AcidO414PZ4LPZACTIB
WATER059QF0KO0RIACT
Sodium Cocoyl Isethionate518XTE8493IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GlycerinPDC6A3C0OXIACT
Sodium Laureth SulfateBPV390UAP0IACT
Sodium Hydroxide55X04QC32IIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
EDETATE DISODIUM7FLD91C86KIACT
LAVANDULA STOECHAS FLOWERING TOP70759G2U6AIACT
HELICHRYSUM ITALICUM FLOWERP62Y550X24IACT

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
24a804b5-7149-44f5-a3b0-70e45250bca9d0f820f7-bd6d-4a18-a9c4-7f0293259bcf2018-06-07WarningsExact identifier
spl id: 24a804b5-7149-44f5-a3b0-70e45250bca9
spl set id: d0f820f7-bd6d-4a18-a9c4-7f0293259bcf

Reported adverse events (FAERS/openFDA)#

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