FDA.reportPublic FDA data

TRIDERMA PAIN RELIEF

Product NDC
10738-073
11-digit product format
107380073
Labeler code
10738
Product ID
10738-073_496701e3-f506-de4f-e063-6294a90a70ff
Type
HUMAN OTC DRUG
Nonproprietary name
Lidocaine HCl, Menthol
Dosage form
CREAM
Route
TOPICAL
Labeler
Genuine Virgin Aloe Corporation
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-08-30
Substance
LIDOCAINE HYDROCHLORIDE; MENTHOL, UNSPECIFIED FORM
Active strength
4; 1 g/100g; g/100g
Pharmacologic classes
Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
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
TRIDERMA PAIN RELIEF
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LIDOCAINE HYDROCHLORIDE4 g/100g
MENTHOL, UNSPECIFIED FORM1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
V13007Z41AInternal UNII lookup
L7T10EIP3AInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1595624Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
9172d6cd-f7d3-421e-a8b5-c1cb3325ada5Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
10738-073-202023-02-02TRIDERMA PAIN RELIEF CREAM
10738-073-412023-02-02TRIDERMA PAIN RELIEF CREAM
10738-073-202023-01-30TRIDERMA PAIN RELIEF CREAM
10738-073-412023-01-30TRIDERMA PAIN RELIEF CREAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10738-073-21TRIDERMA PAIN RELIEF57 g in 1 JARCREAM575
10738-073-41TRIDERMA PAIN RELIEF113 g in 1 JARCREAM1135

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10738-073TRIDERMA PAIN RELIEF (LIDOCAINE HCL, MENTHOL) CREAM [GENUINE VIRGIN ALOE CORPORATION]4Current NDC, Legacy NDC, 2 package rows20250101_9172d6cd-f7d3-421e-a8b5-c1cb3325ada5.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TRIDERMA PAIN RELIEFLIDOCAINE HCL, MENTHOLGenuine Virgin Aloe Corporation9172d6cd-f7d3-421e-a8b5-c1cb3325ada52026-01-27WarningsExact identifier
ndc (product): 10738-073

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1595624lidocaine HCl 4 % / menthol 1 % Topical CreamPSN9172d6cd-f7d3-421e-a8b5-c1cb3325ada55
1595624lidocaine hydrochloride 40 MG/ML / menthol 10 MG/ML Topical CreamSCD9172d6cd-f7d3-421e-a8b5-c1cb3325ada55
1595624lidocaine hydrochloride 4 % / menthol 1 % Topical CreamSY9172d6cd-f7d3-421e-a8b5-c1cb3325ada55

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10738-073-20107380073201 JAR in 1 CARTON (10738-073-20) > 57 g in 1 JAR (10738-073-21) 1 jar2019-08-300000-00-00NoNoCurrent
10738-073-211073800732157 g in 1 JAR (10738-073-21) 57 g2019-08-30NoNoCurrent
10738-073-4110738007341113 g in 1 JAR (10738-073-41) 113 g2019-08-300000-00-00NoNoCurrent