FDA.reportPublic FDA data

Equate Pain Relieving

Product NDC
49035-700
11-digit product format
490350700
Labeler code
49035
Product ID
49035-700_48c4e8c4-4470-75d4-e063-6394a90a4884
Type
HUMAN OTC DRUG
Nonproprietary name
Camphor, Menthol, Methyl salicylate
Dosage form
CREAM
Route
TOPICAL
Labeler
Wal-Mart Stores Inc
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2011-06-13
Substance
CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE
Active strength
40; 100; 300 mg/g; mg/g; mg/g
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
Equate Pain Relieving
Brand name suffix
Ultra Strength
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAMPHOR (SYNTHETIC)40 mg/g
MENTHOL, UNSPECIFIED FORM100 mg/g
METHYL SALICYLATE300 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5TJD82A1ETInternal UNII lookup
L7T10EIP3AInternal UNII lookup
LAV5U5022YInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
283083Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
5ed1d7b3-925e-4a18-8e15-636f5b442ad7Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-700-012023-02-07C16284748780-1f386c649-f0eb-0266-e053-dadaa90a7c1aDrug Facts - Equate Pain Relieving Ultra Strength
49035-700-012023-01-30C16284748780-1f386c649-f0eb-0266-e053-dadaa90a7c1aDrug Facts - Equate Pain Relieving Ultra Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-700-01Equate Pain RelievingUltra Strength113.3 g in 1 TUBECREAM113.36
49035-700-01Equate Pain RelievingUltra Strength1 in 1 CARTONCREAM16

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49035-700-01GM - Gram49035-700bbec1b5a-89df-43e2-a493-26f8a2a479b012013-09-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ETEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
MENTHOLACTIVE INGREDIENTL7T10EIP3AEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022YEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ETEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
MENTHOLACTIVE MOIETYL7T10EIP3AEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
.ALPHA.-TOCOPHEROLINACTIVE INGREDIENTH4N855PNZ1EQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)INACTIVE INGREDIENT4Q93RCW27EEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
COCONUT OILINACTIVE INGREDIENTQ9L0O73W7LEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
EDETATE DISODIUMINACTIVE INGREDIENT7FLD91C86KEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
GLYCERYL MONOSTEARATEINACTIVE INGREDIENT230OU9XXE4EQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
ISOPROPYL MYRISTATEINACTIVE INGREDIENT0RE8K4LNJSEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
LANOLININACTIVE INGREDIENT7EV65EAW6HEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
MINERAL OILINACTIVE INGREDIENTT5L8T28FGPEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
POLYSORBATE 60INACTIVE INGREDIENTCAL22UVI4MEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
TROLAMINEINACTIVE INGREDIENT9O3K93S3TKEQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2
WATERINACTIVE INGREDIENT059QF0KO0REQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-700EQUATE PAIN RELIEVING ULTRA STRENGTH (CAMPHOR, MENTHOL, METHYL SALICYLATE) CREAM [WAL-MART STORES INC]5Current NDC, Legacy NDC, 2 package rows20241219_5ed1d7b3-925e-4a18-8e15-636f5b442ad7.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 90 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Re-Lieved Lidocaine PatchLIDOCAINE PATCH 4%Transfer Technology37ef02d4-2ff5-cb23-e063-6294a90a68af2025-06-19WarningsExact identifier
application number: M017
Post-Treatment Repair CreamHYDROCORTISONEVi Medical Products Inc.ab8885a9-0778-28ff-e053-2995a90a2e122025-06-19WarningsExact identifier
application number: M017
MyDermLIDOCAINEInspec Solutions LLC.82d075d1-c92e-2097-e053-2991aa0ab1312025-06-18WarningsExact identifier
application number: M017
Walgreens Extra Small LidocaineLIDOCAINEWalgreen Co.dc838e47-d234-4ba5-9449-f645e99be9232025-06-18WarningsExact identifier
application number: M017
CLn Body MoisturizerCOLLOIDAL OAT MOISTURIZERTopMD Skin Care, Inc.2de3d68d-a540-d456-e063-6394a90a4b572025-06-18WarningsExact identifier
application number: M017
Aloe UP SPF 30 MineralZINC OXIDE, TITANIUM DIOXIDEAloe Care International, LLC35967b33-bdfb-ee3c-e063-6294a90a75f62025-06-18WarningsExact identifier
application number: M017
Aloe Up SPF 50 MineralZINC OXIDE, TITANIUM DIOXIDEAloe Care International, LLC35b9dcfa-05f3-3d7b-e063-6394a90a18f12025-06-18WarningsExact identifier
application number: M017
Aloe Up SPF 50 MineralZINC OXIDEAloe International, LLC35bc3621-f4e4-42d3-e063-6394a90a7aad2025-06-18WarningsExact identifier
application number: M017
Aloe Up SPF 50 Kids MineralZINC OXIDE, TITANIUM DIOXIDEAloe Care International, LLC35cd16b0-bd81-8f68-e063-6294a90a3d8c2025-06-18WarningsExact identifier
application number: M017
Aloe Up SPF 50 Kids MineralZINC OXIDEAloe International, LLC35cd5542-947d-a042-e063-6394a90a13f82025-06-18WarningsExact identifier
application number: M017
Relieve Your PainMENTHOLProximity Capital Partners LLC dba Asutrac12369dd-8305-edaf-e053-2995a90a0d3d2025-06-18WarningsExact identifier
application number: M017
Melt Pain AwayCAPSAICINProximity Capital Partners LLC dba Asutraa95a11d7-a2ae-6654-e053-2a95a90a802c2025-06-18WarningsExact identifier
application number: M017
Recovery Roll-OnMENTHOL, CAMPHORPROXIMITY CAPITAL PARTNERS LLC DBA ASUTRAebc9630f-6d8b-e4f0-e053-2995a90a0b492025-06-18WarningsExact identifier
application number: M017
ProCure Hydrocortisone 1%HYDROCORTISONETwin Med LLC37cdfabc-1fdb-246a-e063-6394a90a008a2025-06-17WarningsExact identifier
application number: M017
ProCure Hydrocortisone 1%HYDROCORTISONETwin Med LLC37ce6c35-b211-43de-e063-6294a90ab7732025-06-17WarningsExact identifier
application number: M017
Hydrocortisone with AloeHYDROCORTISONE CREAM 1%Sun Pharmaceutical Industries, Inc.312ddc8d-100e-cfac-e063-6294a90acd092025-06-16WarningsExact identifier
application number: M017
Curist 5% LidocaineLIDOCAINE 5%Little Pharma, Inc.f20241a2-c5b1-f124-e053-2995a90a891b2025-06-16WarningsExact identifier
application number: M017
Toast Screamin MentholMENTHOLIDEAZ, LLC37b48b1a-ef3d-afdc-e063-6294a90a66102025-06-16WarningsExact identifier
application number: M017
Toast Freezin ColdMENTHOL, METHYL SALICYLATEIDEAZ, LLC37b4d363-0099-8cd3-e063-6394a90a18d62025-06-16WarningsExact identifier
application number: M017
Earths Care Anti-ItchCAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORMDLC Laboratories, Inc.ba65f58a-d590-498a-b8e7-a3d78935d8802025-06-13WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
283083camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical CreamPSN5ed1d7b3-925e-4a18-8e15-636f5b442ad76
283083camphor 40 MG/ML / menthol 100 MG/ML / methyl salicylate 300 MG/ML Topical CreamSCD5ed1d7b3-925e-4a18-8e15-636f5b442ad76
283083camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical CreamSY5ed1d7b3-925e-4a18-8e15-636f5b442ad76

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-700-01490350700011 TUBE in 1 CARTON (49035-700-01) / 113.3 g in 1 TUBE1 tube2011-06-130000-00-00NoNoCurrent