FDA.reportPublic FDA data

Aspire Cleanser So Fresh

Manufacturer
RNA PHARMA, LLC
Effective date
2021-09-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:42:20

Label at a glance#

ProductAspire Cleanser So Fresh
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
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
60717-311-342025-01-30C16284748780-12cef2736-8ab8-d83d-e063-dadaa90ab31fcb92df75-8cf3-5711-e053-2995a90ab7b2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60717-311-34Aspire Cleanser So Fresh100 mL in 1 TUBEGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60717-311ASPIRE CLEANSER SO FRESH (SALICYLIC ACID) GEL [RNA PHARMA, LLC]1Legacy NDC, 1 package rows20210910_cb92df75-8cf3-5711-e053-2995a90ab7b2.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
60717-31160717-311-34

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
WATER059QF0KO0RIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
EDETATE DISODIUM7FLD91C86KIACT
GLYCERINPDC6A3C0OXIACT
PANTHENOLWV9CM0O67ZIACT
CHAMOMILEFGL3685T2XIACT
ALOE VERA LEAFZY81Z83H0XIACT
SORBITOL506T60A25RIACT
CUCUMBERYY7C30VXJTIACT
SODIUM BENZOATEOJ245FE5EUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S)T967IEU43CIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
LEVOMENOL24WE03BX2TIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
cb92df75-8cf4-5711-e053-2995a90ab7b2cb92df75-8cf3-5711-e053-2995a90ab7b22021-09-09WarningsExact identifier
spl id: cb92df75-8cf4-5711-e053-2995a90ab7b2
spl set id: cb92df75-8cf3-5711-e053-2995a90ab7b2

Reported adverse events (FAERS/openFDA)#

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