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 31 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sunburn Relief GelLIDOCAINE HCLAmazon.com Services LLCadb638ec-4a7c-42f2-b249-0ac53a8dd4b22026-03-03Warnings, Adverse reactionsExact identifier
application number: M017
Aloe Vera GelLIDOCAINE HCL, MENTHOLAmazon.com Services LLC2acb1a6a-57e6-4915-b03a-89d1d2db3baf2026-03-03Warnings, Adverse reactionsExact identifier
application number: M017
Diphenhydramine Hydrochloride and Zinc AcetateDIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATESTRATEGIC SOURCING SERVICES LLCec0c9602-35cc-4bb6-b853-794a8b5bf42e2026-03-03WarningsExact identifier
application number: M017
HYDROCORTISONEHYDROCORTISONE 1%PHARMACY CHOICE INC4cdfe8b6-c332-7bf8-e063-6394a90abaec2026-03-03WarningsExact identifier
application number: M017
HEEL PAIN RELIEF ROLL-ONLIDOCAINE AND MENTHOLGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.4c06c4a4-557b-8bb1-e063-6294a90a91252026-03-02WarningsExact identifier
application number: M017
Sunburn ReliefLIDOCAINE HCL 0.5%Old East Main Co.49173ec8-c94a-44c9-8a13-0f4b01b96cd62026-03-02Warnings, Adverse reactionsExact identifier
application number: M017
Itch ReliefDIPHENHYDRAMINE HCL, ZINC ACETATEOld East Main Co.6d87547f-bf4c-4dda-bd9d-32b576afd8052026-03-02Warnings, Adverse reactionsExact identifier
application number: M017
Still StandingMENTHOL, UNSPECIFIED FORMNatural Essentials Inc.66974aaf-c82f-4fe9-bfb3-3430b80ac9f22026-03-02WarningsExact identifier
application number: M017
Lightning Pain ReliefMENTHOLClinical Resolution Laboratory, Inc.80af21f5-dba8-42b0-8a65-ac5a94d83ca82026-03-02WarningsExact identifier
application number: M017
Icy Hot Lidocaine No-MessLIDOCAINE HYDROCHLORIDEChattem, Inc.347f9a18-8ab6-47d3-9610-5b4e9ca5d53a2026-03-02WarningsExact identifier
application number: M017
Gold Bond Maximum Strength Foot Pain ReliefLIDOCAINE HYDROCHLORIDEGold Bond Co LLC8e469076-2f5a-4de8-8d13-a38c072b9af82026-03-01WarningsExact identifier
application number: M017
HealthWise Pain Relief LidocaineLIDOCAINE HYDROCHLORIDEVeridian Healthcare48ecbab9-13e0-d0fa-e063-6294a90a6ff22026-02-28WarningsExact identifier
application number: M017
NUMBING CREAMSLIDOCAINEYongchun Lihui Trading Co., Ltd.3b5e1a74-5946-4f1f-e063-6394a90a404b2026-02-27WarningsExact identifier
application number: M017
Pain Relieving GelLIDOCAINE HYDROCHLORIDEChain Drug Marketing Associationb55b7253-2fd2-45cc-b94c-e92395ab0d2b2026-02-27Warnings, Adverse reactionsExact identifier
application number: M017
MEDISTIK PROFESSIONAL DUAL ACTIONMENTHOL, METHYL SALICYLATE, EUCALUPTUSNatureteq Inc.99c7f08a-ab14-4371-9147-189f75cb66332026-02-27WarningsExact identifier
application number: M017
Aloe Vera GelLIDOCAINE HCL, MENTHOLWalmart Inc.309dcf5b-7166-976a-e063-6394a90af9522026-02-27Warnings, Adverse reactionsExact identifier
application number: M017
ASYSTEM Radical Relief Gel Roll-OnMENTHOL, METHYL SALICYLATECosco International, Inc.7239733e-5510-4a63-96c3-dd88b4a431a32026-02-27WarningsExact identifier
application number: M017
Icy Hot Pro Pain Massaging BalmCAMPHOR AND MENTHOLChattem, Inc.09e2b0cb-5186-4f9c-b256-edaced4ca0142026-02-27WarningsExact identifier
application number: M017
Lidocaine Pain ReliefLIDOCAINE PAIN RELIEFPAI Holdings, LLC dba PAI Pharma963978de-8295-47ee-9b06-64c3521aa9942026-02-26WarningsExact identifier
application number: M017
Tommie Copper Cooling Roller Lavender ScentMENTHOL 4%Tommie Copper, Inc.4bbfd4d1-9036-bc20-e063-6394a90a3feb2026-02-26WarningsExact 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