Capsaicin 0.035 Percent

Product NDC
50488-1035
11-digit product format
504881035
Labeler code
50488
Product ID
50488-1035_e2a30b7f-bcde-4a77-bcbd-3e965d4f8004
Type
HUMAN OTC DRUG
Nonproprietary name
Capsaicin
Dosage form
CREAM
Route
TOPICAL
Labeler
Alexso, Inc
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-09-01
Substance
CAPSAICIN
Active strength
.035 g/100g
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
Capsaicin 0.035 Percent
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAPSAICIN.035 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
S07O44R1ZMInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
577395Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
6d0bc1cc-e812-4753-b20c-c0357dd6deb5Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50488-1035-1Capsaicin 0.035 Percent120 g in 1 BOTTLECREAM1202

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50488-1035-1GM - Gram50488-103541964388-d8a5-429d-8c3a-dccbbb9de67212026-04-20

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 38 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TheraCare Muscle and Joint Gel Vanishing ScentMENTHOL 2.5%Veridian Healthcare494d2a85-45a8-12a2-e063-6294a90a391b2026-01-26WarningsExact identifier
application number: M017
Lidocaine Pain ReliefLIDOCAINETrifecta Pharmaceuticals USA, LLC.493c09d0-16d7-7413-e063-6394a90aa0522026-01-26WarningsExact identifier
application number: M017
Topcare Medicated Pain Relieving Patch 60ctTOPCARE PAIN RELIEF PATCH EXTRA STRENGTHTopco Associates LLC4953c12b-ca6d-d21e-e063-6294a90ac9902026-01-26WarningsExact identifier
application number: M017
Dr SabharwalsMENTHOL 5% PATCHDr. Sabharwal's Wound Care1025b986-a1e5-701d-e063-6294a90a33fd2026-01-24WarningsExact identifier
application number: M017
Target Up and Up Pain Relief Menthol Topical AnalgesicMENTHOLTarget Corporation4910f32f-c639-0215-e063-6394a90a1c7b2026-01-23WarningsExact identifier
application number: M017
RapidolHYDROCORTISONEPharmadel LLC19a1f1e2-bc6b-7153-e063-6294a90ab1152026-01-23WarningsExact identifier
application number: M017
CVS 9083 Maximum Strength Lidocaine 4 Pain Relief Patch 1ct LargeLIDOCAINECVS PHARMACY, INC4914965f-1164-e20e-e063-6294a90ac2212026-01-23WarningsExact identifier
application number: M017
THE GOO MEDICATED PAIN RELIEFMETHYL SALICYLATE, MENTHOL, CAMPHORAPSM PERFORMANCE, LLCdb4c321c-8cdc-5a11-e053-2995a90a91a12026-01-23WarningsExact identifier
application number: M017
Dr SabharwalsLIDOCAINE 4% AND MENTHOL 1% PATCHDr. Sabharwal's Wound Care10249d0f-5ee1-6892-e063-6394a90a967e2026-01-23WarningsExact identifier
application number: M017
Easment DMSO creamMENTHOL 1.00%Easment LLC48f5544e-1cfd-864a-e063-6394a90a71f12026-01-22WarningsExact identifier
application number: M017
Aveeno 1% Hydrocortisone Anti-Itch CreamHYDROCORTISONEKenvue Brands LLC1ac0ac4e-af76-9a3e-e063-6394a90a12692026-01-22WarningsExact identifier
application number: M017
RAYO ACTIVE ICEMENTHOL, CAMPHORQuimicas Handal de Centroamerica SA de CV09e4a36b-020a-c5b1-e063-6394a90a3e312026-01-22WarningsExact identifier
application number: M017
X-Treme FreezeCOLD THERAPY GELDynarex Corporation79f0802f-03ad-bf8f-e053-2991aa0ae4b52026-01-22WarningsExact identifier
application number: M017
Anti ItchHYDROCORTISONEHyVee Incae31f1f5-db70-45cf-850e-67bfe68607482026-01-21WarningsExact identifier
application number: M017
ULTRA RELIEFMENTHOL, CAMPHORCHEMCO CORPORATION48ea80cf-af54-ce5f-e063-6394a90ac4932026-01-21WarningsExact identifier
application number: M017
Healthy Back Institute Rub On ReliefANALGESICEagle Labs Inc.17dff3c1-3c0b-16f6-e063-6394a90a3c052026-01-21WarningsExact identifier
application number: M017
Pain ReliefANALGESICFullstack Fulfillment2a433cee-8b6f-c280-e063-6394a90ae25a2026-01-21Exact identifier
application number: M017
Walgreens Anti Itch CreamANTI ITCH CREAMWalgreens Companyb545553a-283a-48af-adc5-763758a9ff242026-01-21WarningsExact identifier
application number: M017
CVS Health Maximum Strength Lidocaine Pain Relief Cream Plus MentholLIDOCAINE HCL, MENTHOLCVS Pharmacy8aaffa3f-f82f-470c-902d-f366f1a663052026-01-21WarningsExact identifier
application number: M017
LIGHTS Instant Sting Relief PadBENZOCAINELights Medical Manufacture Co., Ltd.28dd82a7-f360-a022-e063-6394a90a3a762026-01-21WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
577395capsaicin 0.035 % Topical CreamPSN6d0bc1cc-e812-4753-b20c-c0357dd6deb52
577395capsaicin 0.35 MG/ML Topical CreamSCD6d0bc1cc-e812-4753-b20c-c0357dd6deb52
577395capsaicin 0.035 % Topical CreamSY6d0bc1cc-e812-4753-b20c-c0357dd6deb52

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
50488-1035-150488103501120 g in 1 BOTTLE (50488-1035-1) 120 g2025-09-01NoNoCurrent