FDA.reportPublic FDA data

Aspire Scrub So Clean

Manufacturer
RNA PHARMA, LLC
Effective date
2021-09-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:42:19

Label at a glance#

ProductAspire Scrub So Clean
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredientsactive ingredients

DOSAGE & ADMINISTRATION SECTION

dosage & administrationdosage & administration

WARNINGS SECTION

warningswarnings

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

INDICATIONS & USAGE SECTION

indications & usageindications & usage

OTC - PURPOSE SECTION

purposepurpose

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label principalpackage label principal

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
865105salicylic acid 0.5 % Medicated Liquid SoapPSN1
865105salicylic acid 5 MG/ML Medicated Liquid SoapSCD1
865105salicylic acid 0.5 % Foaming CleanserSY1
865105salicylic acid 0.5 % MaskSY1
865105salicylic acid 0.5 % Medicated Liquid SoapSY1
865105salicylic acid 0.5 % Topical Gel CleanserSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60717-310-342025-01-30C16284748780-12cef2736-b105-d83d-e063-dadaa90ab31fcb8234c4-c548-4b67-e053-2995a90af7d9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60717-310-34Aspire Scrub So Clean100 mL in 1 TUBELOTION1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60717-310ASPIRE SCRUB SO CLEAN (SALICYLIC ACID) LOTION [RNA PHARMA, LLC]1Legacy NDC, 1 package rows20210909_cb8234c4-c548-4b67-e053-2995a90af7d9.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60717-31060717-310-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
SODIUM COCOAMPHOACETATEW7Q5E87674IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PANTHENOLWV9CM0O67ZIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
ALOE VERA LEAFZY81Z83H0XIACT
DISODIUM LAURETH SULFOSUCCINATED6DH1DTN7EIACT
CHROMIUM HYDROXIDE GREENRV8FT8XF5RIACT
RICE BRANR60QEP13ICIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
EDETATE DISODIUM7FLD91C86KIACT
LEVOMENOL24WE03BX2TIACT
CHAMOMILEFGL3685T2XIACT
SORBITOL506T60A25RIACT
CUCUMBERYY7C30VXJTIACT
GLYCERINPDC6A3C0OXIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
SALICYLIC ACIDO414PZ4LPZACTIB
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
cb8234c4-c549-4b67-e053-2995a90af7d9cb8234c4-c548-4b67-e053-2995a90af7d92021-09-08WarningsExact identifier
spl id: cb8234c4-c549-4b67-e053-2995a90af7d9
spl set id: cb8234c4-c548-4b67-e053-2995a90af7d9

Reported adverse events (FAERS/openFDA)#

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