FDA.reportPublic FDA data

Pain Away

Product NDC
79804-265
Requested package NDC
79804-265-08
11-digit product format
798040265
Labeler code
79804
Product ID
79804-265_ec58d29b-d048-0a7d-e053-2a95a90a8761
Type
HUMAN OTC DRUG
Nonproprietary name
Analgesic
Dosage form
SPRAY
Route
TOPICAL
Labeler
Eagle Labs Inc.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-07-01
Marketing end
0000-00-00
Substance
CAMPHOR (SYNTHETIC); CAPSAICIN; MENTHOL
Active strength
0 g/g; g/g; g/g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage79804-26579804-265-08IInactivated by FDA2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage79804-26579804-265-08IInactivated by FDAexcluded / ndc_excluded.zip1332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
79804-265-042026-01-29Pain Spray Extra Strength
79804-265-082026-01-29Pain Spray Extra Strength
79804-265-042024-04-16Pain Spray Extra Strength
79804-265-082024-04-16Pain Spray Extra Strength
79804-265-042024-01-30Pain Spray Extra Strength
79804-265-082024-01-30Pain Spray Extra Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79804-265-04Pain Away108 g in 1 BOTTLE, PLASTICSPRAY1084
79804-265-08Pain Away216 g in 1 BOTTLE, PLASTICSPRAY2164

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79804-265PAIN AWAY (ANALGESIC) SPRAY [EAGLE LABS INC.]4Legacy NDC, 2 package rows20240418_3de88c3b-0302-4005-8029-98364c6257f7.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2609762camphor 11 % / capsaicin 0.1 % / menthol 16 % Topical SprayPSN3de88c3b-0302-4005-8029-98364c6257f74
2609762camphor 110 MG/ML / capsaicin 1 MG/ML / menthol 160 MG/ML Topical SpraySCD3de88c3b-0302-4005-8029-98364c6257f74
2609762camphor 11 % / capsaicin 0.1 % / menthol 16 % Topical SpraySY3de88c3b-0302-4005-8029-98364c6257f74

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79804-265-0879804026508216 g in 1 BOTTLE, PLASTIC (79804-265-08) 216 g2022-07-010000-00-00NoNoCurrent