FDA.reportPublic FDA data

Aspire Treat So Deep

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 23:42:21

Label at a glance#

ProductAspire Treat So Deep
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
346298salicylic acid 2 % Topical GelPSN1
346298salicylic acid 0.02 MG/MG Topical GelSCD1
346298salicylic acid 2 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60717-312-052025-01-30C16284748780-12cef2736-6bd4-d83d-e063-dadaa90ab31fcb93fd98-bea8-39dd-e053-2a95a90ac962

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60717-312-05Aspire Treat So Deep15 mL in 1 TUBEGEL151
60717-312-05Aspire Treat So Deep1 in 1 BOXGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60717-312ASPIRE TREAT SO DEEP (SALICYLIC ACID) GEL [RNA PHARMA, LLC]1Legacy NDC, 2 package rows20210911_cb93fd98-bea8-39dd-e053-2a95a90ac962.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60717-31260717-312-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
EDETATE DISODIUM7FLD91C86KIACT
SODIUM CITRATE1Q73Q2JULRIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CAPRYLYL GLYCOL00YIU5438UIACT
OLEANOLIC ACID6SMK8R7TGJIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
ALCOHOL3K9958V90MIACT
LEVOMENOL24WE03BX2TIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
TETRAHEXYLDECYL ASCORBATE9LBV3F07AZIACT
SODIUM HYDROXIDE55X04QC32IIACT
PEG-8/SMDI COPOLYMERCCX72L6NY6IACT
SACCHARIDE ISOMERATEW8K377W98IIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PEG-60 ALMOND GLYCERIDES4Y0E651N0FIACT
ALLANTOIN344S277G0ZIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
DIMETHYL ISOSORBIDESA6A6V432SIACT
NORDIHYDROGUAIARETIC ACID, (+/-)-7PZ73W4ZNRIACT

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
cb93fd98-bea9-39dd-e053-2a95a90ac962cb93fd98-bea8-39dd-e053-2a95a90ac9622021-09-09WarningsExact identifier
spl id: cb93fd98-bea9-39dd-e053-2a95a90ac962
spl set id: cb93fd98-bea8-39dd-e053-2a95a90ac962

Reported adverse events (FAERS/openFDA)#

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