FDA.reportPublic FDA data

Thayers Blemish Clearing Balm

Manufacturer
RNA PHARMA, LLC
Effective date
2021-02-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:58

Label at a glance#

ProductThayers Blemish Clearing Balm
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
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
60717-011-042025-01-30C16284748780-12cef2736-796d-d83d-e063-dadaa90ab31fbbdfcf0d-295f-f6d6-e053-2a95a90a4c42

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60717-011-04Thayers Blemish Clearing Balm1 in 1 TUBELOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60717-011THAYERS BLEMISH CLEARING BALM (SALICYLIC ACID) LOTION [RNA PHARMA, LLC]1Legacy NDC, 1 package rows20210313_bbdfcf0d-295f-f6d6-e053-2a95a90a4c42.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60717-01160717-011-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
EAST INDIAN LEMONGRASS OILUP0M8M3VZWIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
XANTHAN GUMTTV12P4NEEIACT
CARRAGEENAN5C69YCD2YJIACT
PEG-100 STEARATEYD01N1999RIACT
HAMAMELIS VIRGINIANA TOPUDA30A2JJYIACT
SALICYLIC ACIDO414PZ4LPZACTIB
SUNFLOWER OIL3W1JG795YIIACT
STEARIC ACID4ELV7Z65APIACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
WHITE WAX7G1J5DA97FIACT
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
TEA TREE OILVIF565UC2GIACT

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
bbdfcf0d-2960-f6d6-e053-2a95a90a4c42bbdfcf0d-295f-f6d6-e053-2a95a90a4c422021-02-21WarningsExact identifier
spl id: bbdfcf0d-2960-f6d6-e053-2a95a90a4c42
spl set id: bbdfcf0d-295f-f6d6-e053-2a95a90a4c42

Reported adverse events (FAERS/openFDA)#

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