Sombra Max

Product NDC
61577-3440
11-digit product format
615773440
Labeler code
61577
Product ID
61577-3440_41623a46-e6e8-907e-e063-6394a90afc4c
Type
HUMAN OTC DRUG
Nonproprietary name
Sombra Max
Dosage form
CREAM
Route
TOPICAL
Labeler
Sombra Cosmetics Inc.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-01-01
Substance
MENTHOL GLUCURONIDE; HISTAMINE DIHYDROCHLORIDE; CAMPHOR (SYNTHETIC); CAPSAICIN; METHYL SALICYLATE
Active strength
6; .025; 3; .025; 12 g/100g; g/100g; g/100g; g/100g; 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
Sombra Max
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL GLUCURONIDE6 g/100g
HISTAMINE DIHYDROCHLORIDE.025 g/100g
CAMPHOR (SYNTHETIC)3 g/100g
CAPSAICIN.025 g/100g
METHYL SALICYLATE12 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
WW64GZ6LQYInternal UNII lookup
3POA0Q644UInternal UNII lookup
5TJD82A1ETInternal UNII lookup
S07O44R1ZMInternal UNII lookup
LAV5U5022YInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
41623a46-e6e7-907e-e063-6394a90afc4cAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61577-3440-1Sombra Max1 g in 1 CONTAINERCREAM11
61577-3440-2Sombra Max1 g in 1 PACKETCREAM11

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 50 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Amazon Basics Pain Relief Patch with 4% LidocaineLIDOCAINEAmazon.com Services LLCe3b4f9b1-ac6b-cb2a-e053-2a95a90a9e1e2025-12-28WarningsExact identifier
application number: M017
Absorbine Jr Neck and ShoulderABSORBINE JR NECK AND SHOULDERClarion Brands LLC22f2f191-9146-3075-e063-6394a90aef5f2025-12-28WarningsExact identifier
application number: M017
Absorbine Jr. Pain Relieving Knee PatchABSORBINE JR. PAIN RELIEVING KNEE PATCHClarion Brands, LLC22f71254-e521-2d82-e063-6394a90a12d82025-12-28WarningsExact identifier
application number: M017
Absorbine Jr Back PatchABSORBINE JR BACK PATCHClarion Brands LLC.22f5147e-ff2b-4ae8-e063-6394a90a4e542025-12-28WarningsExact identifier
application number: M017
Absorbine Jr. Pro RollonABSORBINE JR. PRO ROLLONClarion Brands, LLC470efcd0-d350-3dc4-e063-6394a90ab8c12025-12-28WarningsExact identifier
application number: M017
Med Rub BalmACHES AND PAIN BALMWellmetech Pharmaceutical Industries SDN BHDa5801566-6bbe-44f6-8761-9c1ce30969002025-12-27WarningsExact identifier
application number: M017
N-Labs ArcticZen Pain Relief KneeCAMPHOR (SYNTHETIC), MENTHOLNutriomo Labs PTE., LTD46e92db7-a48b-2c7a-e063-6394a90a438e2025-12-27WarningsExact identifier
application number: M017
Absorbine Jr. PlusMENTHOLClarion Brands, LLC46f4ad3c-7418-a6bf-e063-6394a90a4eb82025-12-27WarningsExact identifier
application number: M017
Equate Lidocaine Cool and HeatLIDOCAINE 4% PLUS MENTHOL 1%Walmart Stores Incb86769c3-a0b4-c481-e053-2a95a90af38b2025-12-27WarningsExact identifier
application number: M017
Medicated Body Extra Strength PowderMENTHOL 0.80%Walmart Stores Incb0786418-7b28-d316-e053-2995a90a3ab52025-12-27WarningsExact identifier
application number: M017
Maximum Strength Medicated Foot PowderMEDICATED FOOT POWDERWalmart Stores Incb0794d48-eb8b-55c9-e053-2995a90a5b382025-12-27WarningsExact identifier
application number: M017
Walgreens 24-Hour Lidocaine PatchLIDOCAINE 4%Walgreens Companyb8402924-b5fc-0acd-e053-2a95a90a18052025-12-27WarningsExact identifier
application number: M017
Frankincense and Myrrh Foot Pain ReliefMENTHOLWISE CONSUMER PRODUCTS CO.115f1abc-34aa-3c20-e063-6294a90a97642025-12-26WarningsExact identifier
application number: M017
Soothing Nerve ReliefMENTHOLWise Consumer Products46e23c95-1a36-214e-e063-6394a90a98a82025-12-26WarningsExact identifier
application number: M017
Frankincense and Myrrh Foot Pain Relief Combo PackMENTHOLWISE CONSUMER PRODUCTS CO.46e2c8b6-bd94-7100-e063-6294a90ac9982025-12-26WarningsExact identifier
application number: M017
Pain Patch Perfecto 24 Hours Lidocaine 4 % PatchLIDOCAINEPainpatchperfecto LLCa281c3e9-1c48-4905-98cc-3cedf6042adc2025-12-25WarningsExact identifier
application number: M017
Aloe UP SPF 33 MineralZINC OXIDEAloe Care International, LLC35aa6196-682d-8f32-e063-6394a90aad992025-12-24WarningsExact identifier
application number: M017
ETADERM Numbing CreamLIDOCAINENUEPHASE LLC5292c6ff-b878-4e71-878b-4bf08207612e2025-12-24WarningsExact identifier
application number: M017
Certain Dri Clinical Strength Prescription Protection RollonCERTAIN DRI CLINICAL STRENGTH PRESCRIPTION PROTECTION ROLLONClarion Brands LLC46a1f92e-4411-3989-e063-6394a90a70382025-12-23WarningsExact identifier
application number: M017
PREMIERES PAINMENTHOLPremiere Enterprises128bd1e7-e961-416c-933b-fbd146e3d3862025-12-23WarningsExact identifier
application number: M017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
61577-3440-1615773440011 g in 1 CONTAINER (61577-3440-1) 1 g2026-01-01NoNoCurrent
61577-3440-2615773440021 g in 1 PACKET (61577-3440-2) 1 g2026-01-01NoNoCurrent