FDA.reportPublic FDA data

Bleackhead removing Medicated scrub

Manufacturer
Rite Aid | Product Quest Mfg
Effective date
2018-05-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:38

Label at a glance#

ProductBleackhead removing Medicated scrub Daylogic
Active ingredientSalicylic Acid
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                                 Purpose
Salicylic acid 2%..................................................Acne Medication

INDICATIONS & USAGE SECTION

Uses For the treatment of acne and helps clear blackheads

WARNINGS SECTION

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

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

DOSAGE & ADMINISTRATION SECTION

Directions • wet face • gently massage product all over face for 20-30 seconds, avoiding eye area • rinse thoroughly and
pat dry • recommended for daily use

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Cetyl Alcohol, PPG-15
Stearyl Ether, Microcrystalline Wax, Jojoba Esters, Steareth-21,
Polysorbate 60, Ferric Ferrocyanide, Xanthan Gum, Potassium
Cetyl Phosphate, Fragrance, Menthyl Lactate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
103568salicylic acid 2 % Topical LotionPSN1
103568salicylic acid 20 MG/ML Topical LotionSCD1
103568salicylic acid 2 % Topical LotionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-7798-42020-01-31C16284748780-19d75b9cf-cf44-f424-e053-dadaa90a57ced3781871-a2e4-43b4-92df-668aee6163bb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-7798-4Bleackhead removing Medicated scrubDaylogic141 g in 1 TUBELOTION1411

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-7798BLEACKHEAD REMOVING MEDICATED SCRUB DAYLOGIC (SALICYLIC ACID 2.00%) LOTION [RITE AID]1Legacy NDC, 1 package rows20180522_d3781871-a2e4-43b4-92df-668aee6163bb.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-779811822-7798-4

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
Salicylic AcidO414PZ4LPZACTIB
Water059QF0KO0RIACT
Cetyl Alcohol936JST6JCNIACT
PPG-15 Stearyl Ether1II18XLS1LIACT
Microcrystalline WaxXOF597Q3KYIACT
HYDROGENATED JOJOBA OIL, RANDOMIZEDQ47ST02F58IACT
Steareth-2153J3F32P58IACT
Polysorbate 60CAL22UVI4MIACT
Ferric FerrocyanideTLE294X33AIACT
Xanthan GumTTV12P4NEEIACT
Potassium Cetyl Phosphate03KCY6P7UTIACT
MENTHYL LACTATE, (-)-2BF9E65L7IIACT

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
0ae1bbe9-9213-4bfb-97b4-5225addd5f07d3781871-a2e4-43b4-92df-668aee6163bb2018-05-22WarningsExact identifier
spl id: 0ae1bbe9-9213-4bfb-97b4-5225addd5f07
spl set id: d3781871-a2e4-43b4-92df-668aee6163bb

Reported adverse events (FAERS/openFDA)#

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