FDA.reportPublic FDA data

Melt Pain Away

Manufacturer
Proximity Capital Partners LLC dba Asutra | BioLyte Laboratories, LLC
Effective date
2025-06-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:03:26

Label at a glance#

ProductMelt Pain Away
Active ingredientCAPSAICIN
Label structure9 sections

Storage and handling

Store in a cool, dry place. Keep away from excessive heat or flame. Tamper-evident for your protection. Use only if safety seal is intact

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Capsaicin .025%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with:

  • arthritis
  • simple backache
  • strains
  • sprains
  • bruises

WARNINGS SECTION

Use only as directed.

For external use only.

OTC - WHEN USING SECTION

When using this product:

  • avoid contact with eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

OTC - STOP USE SECTION

Stop use and ask doctor if:

  • condition worsens
  • symptoms persist for more than 7 days, or clear up and reoccur again with a few days
  • redness is present
  • irritation develops.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding,ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If accidentally ingested, get medical help or contact Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Adults and children over 18 years:

  • Apply to affected area. Massage into the painful area until thoroughly absorbed. Repeat as necessary but no more than 3 to 4

times daily.

  • Wash hands with soap and water after applying.

Children 18 years and younger:

  • Consult a doctor.

STORAGE AND HANDLING SECTION

  • Store in a cool, dry place.
  • Keep away from excessive heat or flame.
  • Tamper-evident for your protection. Use only if safety seal is intact

INACTIVE INGREDIENT SECTION

Water, Magnesium Chloride, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Cetearyl Alcohol, Butyrospermum Parkii (Shea) Butter, Dimethyl Sulfone (MSM), Sodium Lactate, Glyceryl Stearate Citrate, Cetyl Palmitate, Glycerin, Glyceryl Stearate, Polyglyceryl-3 Diisostearate, Pentylene Glycol, Undecane, Xanthan Gum, Magnesium Sulfate, Tridecane, Potassium Chloride, Sodium Chloride, Calcium Chloride, Tocopheryl Acetate (Vitamin E), Hydroxyacetophenone, Panthenol, Allantoin, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate, Sodium Hydroxide, Cymbopogon Flexuosus (East-Indian Lemongrass) Oil* *Organic

OTC - QUESTIONS SECTION

888-819-6472; Monday–Friday, 9am–5pm CT
Report any serious side effects to number above.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Melt Pain AwayMelt Pain Away

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198555capsaicin 0.025 % Topical CreamPSN3
198555capsaicin 0.25 MG/ML Topical CreamSCD3
198555capsaicin 0.025 % Topical CreamSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
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5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72683-003-012024-08-13C16284748780-11e7a6dab-1f32-a2ce-e063-dadaa90aadf7Melt Pain Away (Asutra)
72683-003-022024-08-13C16284748780-11e7a6dab-1f32-a2ce-e063-dadaa90aadf7Melt Pain Away (Asutra)
72683-003-012024-07-30C16284748780-11e7a6dab-1f32-a2ce-e063-dadaa90aadf7Melt Pain Away (Asutra)
72683-003-022024-07-30C16284748780-11e7a6dab-1f32-a2ce-e063-dadaa90aadf7Melt Pain Away (Asutra)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72683-003-01Melt Pain Away200 g in 1 JARCREAM2003
72683-003-02Melt Pain Away1.9 g in 1 PACKETCREAM1.93

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72683-00372683-003-01, 72683-003-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETOSTEARYL ALCOHOL2DMT128M1SIACT
SODIUM LACTATETU7HW0W0QTIACT
CETYL PALMITATE5ZA2S6B08XIACT
POLYGLYCERYL-3 DISTEARATEZI1LK470XVIACT
MAGNESIUM SULFATE, UNSPECIFIEDDE08037SABIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
PANTHENOLWV9CM0O67ZIACT
SODIUM HYDROXIDE55X04QC32IIACT
CYMBOPOGON FLEXUOSUS LEAF7LJ4Y1UJG7IACT
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)255PIF62MSIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
SHEA BUTTERK49155WL9YIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
UNDECANEJV0QT00NUEIACT
XANTHAN GUMTTV12P4NEEIACT
TRIDECANEA3LZF0L939IACT
POTASSIUM CHLORIDE660YQ98I10IACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALMOND OIL66YXD4DKO9IACT
PENTYLENE GLYCOL50C1307PZGIACT
SODIUM CHLORIDE451W47IQ8XIACT
ALLANTOIN344S277G0ZIACT
WATER059QF0KO0RIACT
CAPSAICINS07O44R1ZMACTIB

Source Document#

Source XML

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
Melt Pain AwayCAPSAICINProximity Capital Partners LLC dba Asutraa95a11d7-a2ae-6654-e053-2a95a90a802c2025-06-18WarningsExact identifier
ndc (package): 72683-003-02
ndc (package): 72683-003-01
ndc (product): 72683-003
ndc11 (package): 72683000302
ndc11 (package): 72683000301
spl id: 37da3909-1e23-f5d9-e063-6294a90a8f48
spl set id: a95a11d7-a2ae-6654-e053-2a95a90a802c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.