SORARESAL

Product NDC
73526-002
11-digit product format
735260002
Labeler code
73526
Product ID
73526-002_d43790bf-7043-408e-829f-08edb70ffdbd
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic Acid
Dosage form
CREAM
Route
TOPICAL
Labeler
Summer Herbal Inc.
Application
M032
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-01-01
Substance
SALICYLIC ACID
Active strength
2 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
SORARESAL
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID2 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O414PZ4LPZInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
317152Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
af734362-057b-4011-bf4e-c4e4dd67f68cAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73526-002-02SORARESAL1 in 1 BOXCREAM112
73526-002-02SORARESAL50 g in 1 BOTTLECREAM5012
73526-002-06SORARESAL1 in 1 BOXCREAM112
73526-002-06SORARESAL191 g in 1 BOTTLECREAM19112

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73526-002SORARESAL (SALICYLIC ACID) CREAM [SUMMER HERBAL INC.]12Current NDC, Legacy NDC, 4 package rows20240911_af734362-057b-4011-bf4e-c4e4dd67f68c.zip

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 31 of 31 · 615 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sulfur 8 Light Anti-Dandruff Hair and Scalp ConditionerSULFURJ. Strickland & Co.d8f9afe8-bc44-41be-806b-b77d2def0fb02023-10-21WarningsExact identifier
application number: M032
Glovers Dandruff Control Medicine, RegularSULFURJ. Strickland & Co.18700036-11ec-4370-bcc6-b9e2c732e7d92023-10-21WarningsExact identifier
application number: M032
Glovers Medicated Anti-Dandruff ScalpSALICYLIC ACIDJ. Strickland & Co.bdf40a16-7b40-497e-939d-366cbe62b5552023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Original Anti-Dandruff Hair and Scalp ConditionerSULFURJ. Strickland & Co.eb1d6e9e-e7fd-478e-80c0-3a3f529682d72023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Loc Twist and Braid ScalpSALICYLIC ACIDJ. Strickland & Co.1aee59aa-ed8e-4f95-be99-63ce0814c03c2023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Fresh Anti-Dandruff Hair and Scalp ConditionerSALICYLIC ACIDJ. Strickland & Co.27b6276a-eaa0-4fb7-996c-53e8c28680912023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff ControlSALICYLIC ACIDJ. Strickland and Co.961ffab9-4e1b-83f3-e053-2a95a90af5fe2023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing TreatmentSALICYLIC ACIDJ. Strickland and Co.96b24a6f-3d6e-6d60-e053-2a95a90a83302023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Oil SerumSULFURJ. Strickland and Co.96b249a2-3f50-1ab8-e053-2995a90a56ed2023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Butter CreamSULFUR, SALICYLIC ACIDJ. Strickland and Co.96b26d20-d4d8-1bc3-e053-2995a90afec02023-10-21WarningsExact identifier
application number: M032
Glovers Clinical Care Seborrheic Dermatitis AntidandruffPYRITHIONE ZINCJ. Strickland and Co.fef5701f-c5c7-4932-9a1c-42532e3910a52023-10-21WarningsExact identifier
application number: M032
Topco AssociatesSELENIUM SULFIDETopco Associatesecf87660-f552-1f6b-e053-2a95a90a24862023-05-04WarningsExact identifier
application number: M032
Careone Medicated DandruffSELENIUM SULFIDERetail Business Services, LLCcb05b9c6-c1bb-b210-e053-2a95a90afaea2021-08-26WarningsExact identifier
application number: M032
GoodSense Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-DandruffSELENIUM SULFIDEGOODSENSE21291e29-57ab-4761-8e8c-eef43ca65b242020-06-30WarningsExact identifier
application number: M032
ZolidynePYRITHIONE ZINCTopiderm, Inc.6d5eaecc-a3a1-4739-ae5b-66df4a15cd212019-11-20WarningsExact identifier
application number: M032

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
317152salicylic acid 2 % Topical CreamPSNaf734362-057b-4011-bf4e-c4e4dd67f68c12
317152salicylic acid 20 MG/ML Topical CreamSCDaf734362-057b-4011-bf4e-c4e4dd67f68c12
317152salicylic acid 2 % Topical CreamSYaf734362-057b-4011-bf4e-c4e4dd67f68c12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73526-002-02735260002021 BOTTLE in 1 BOX (73526-002-02) / 50 g in 1 BOTTLE1 bottle2021-10-010000-00-00NoNoCurrent
73526-002-06735260002061 BOTTLE in 1 BOX (73526-002-06) / 191 g in 1 BOTTLE1 bottle2020-09-160000-00-00NoNoCurrent