PAIN RELIEF Gel-Tube

Product NDC
73557-323
11-digit product format
735570323
Labeler code
73557
Product ID
73557-323_1738d740-3d2c-d509-e063-6394a90a6530
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-12-28
Substance
MENTHOL
Active strength
.04 g/mL
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
PAIN RELIEF Gel-Tube
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL.04 g/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L7T10EIP3AInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
415974Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
f0bec1d4-2e18-4519-e053-2a95a90a1bbbAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73557-323-30PAIN RELIEF Gel-Tube89 mL in 1 TUBEGEL892

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73557-323PAIN RELIEF GEL-TUBE (MENTHOL) GEL [SHANGHAI CHUANGSHI MEDICAL TECHNOLOGY (GROUP) CO., LTD.]2Current NDC, Legacy NDC, 1 package rows20240430_f0bec1d4-2e18-4519-e053-2a95a90a1bbb.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 111 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HealthWise Medicated Original Body Powder 10 ozMENTHOLVeridian Healthcare296b623a-14cd-0bca-e063-6394a90ac5ff2024-12-16WarningsExact identifier
application number: M017
HealthWise Medicated Extra Body Powder 10 ozMENTHOLVeridian Healthcare296c9a9c-e3db-59fe-e063-6294a90a0b622024-12-16WarningsExact identifier
application number: M017
Rite Aid Hot and Cold Roll OnMENTHOL 16%Rite Aidfc4b2635-280b-267f-e053-6294a90a5e222024-12-15WarningsExact identifier
application number: M017
Rite Aid Pain RelievingBENZOCAINE 20%, MENTHOL 0.5%Rite Aide2c09e85-be0a-4e6d-e053-2995a90ad7562024-12-15WarningsExact identifier
application number: M017
Rugby LidocaineLIDOCAINE 4%Rugby Laboratoriesd94292f7-10fc-48bf-e053-2995a90a84722024-12-15WarningsExact identifier
application number: M017
Rite Aid CortisoneHYDROCORTISONE 1%Rite Aide27353b9-23b6-3801-e053-2a95a90a60452024-12-15WarningsExact identifier
application number: M017
Rite Aid Cooling Pain ReliefMENTHOL 10.5%Rite Aide2225259-70ec-52de-e053-2a95a90a73f82024-12-15WarningsExact identifier
application number: M017
Rite Aid Rectal CareLIDOCAINE 5%Rite Aide283e462-96e8-04cf-e053-2a95a90a1d002024-12-15WarningsExact identifier
application number: M017
Rite Aid Anti-ItchDIPHENHYDRAMINE HCL 2%Rite Aide33898d8-1b8b-5c0b-e053-2995a90add082024-12-15WarningsExact identifier
application number: M017
Rite Aid Cala Itch ReliefPRAMOXINE HCL 1%, ZINC ACETATE 0.1%Rite Aide29a9d59-4c7c-81aa-e053-2995a90a70562024-12-15WarningsExact identifier
application number: M017
CVS Roll-OnCAPSAISIN 0.1%CVSe8812c49-335e-61ea-e053-2995a90a17aa2024-12-15WarningsExact identifier
application number: M017
Good Sense Burn Relief AloeLIDOCAINE HCLGeiss, Destin & Dunn, Incb5a7f629-a88d-b49d-e053-2995a90a49fa2024-12-15WarningsExact identifier
application number: M017
QC Burn Relief AloeLIDOCAINE HCLChain Drug Marketing Association Incb5e76f0c-0bfe-b13e-e053-2995a90a08612024-12-15WarningsExact identifier
application number: M017
Meijer Burn ReliefLIDOCAINE 0.5%Meijerbec60c93-5abd-ee04-e053-2a95a90acb612024-12-15WarningsExact identifier
application number: M017
QC Cool and Heat Roll-OnMENTHOL 16%Chain Drug Marketing Association Incd35e9dfa-8a28-fdb3-e053-2995a90abc522024-12-15WarningsExact identifier
application number: M017
Meijer Cold and Hot Pain RelievingMENTHOL 16%Meijerbec62df3-06c9-a115-e053-2995a90a42672024-12-15WarningsExact identifier
application number: M017
Tommie Copper Pain ReliefMENTHOL 16%Tommie Copper, Inc.b4dfa5fa-2d61-db1e-e053-2a95a90a7ac82024-12-15WarningsExact identifier
application number: M017
Pain Relief Liquid RollerCAMPHOR 3.5%, MENTHOL 3.5%Tommie Copper, Inc.c9f0447e-de43-16a5-e053-2995a90a05c12024-12-15WarningsExact identifier
application number: M017
Tommie Copper Pain Relief Maximum StrengthTROLAMINE SALICYLATE 10%Tommie Copper, Inc.b622c14f-9bf3-0bbd-e053-2a95a90a2adc2024-12-15WarningsExact identifier
application number: M017
Copperlife Pain ReliefTROLAMINE SALICYLATE 10%Tommie Copper, Inc.c94d00f9-42ce-1d43-e053-2a95a90a058d2024-12-15WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSNf0bec1d4-2e18-4519-e053-2a95a90a1bbb2
415974menthol 0.04 MG/MG Topical GelSCDf0bec1d4-2e18-4519-e053-2a95a90a1bbb2
415974menthol 4 % Topical GelSYf0bec1d4-2e18-4519-e053-2a95a90a1bbb2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73557-323-307355703233089 mL in 1 TUBE (73557-323-30) 89 ml2022-12-280000-00-00NoNoCurrent