Everlight Survival Sting Relief Pad

Product NDC
72459-022
11-digit product format
724590022
Labeler code
72459
Product ID
72459-022_36c40404-fe90-6fb7-e063-6394a90a2657
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOCAINE
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Yiwu Ori-Power Medtech Co.,Ltd.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-06-02
Substance
BENZOCAINE; ALCOHOL
Active strength
6; 60 g/100g; g/100g
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
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
Everlight Survival Sting Relief Pad
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE6 g/100g
ALCOHOL60 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U3RSY48JW5Internal UNII lookup
3K9958V90MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1046313Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
364c9882-339e-fe22-e063-6294a90a37f4Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72459-022-01Everlight Survival Sting Relief Pad0.8 g in 1 PATCHSOLUTION0.82

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 88 of 151 · 3,010 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hilook Blue Gel AnestheticLIDOCAINEGuangdong Aimu Biological Technology Co., Ltd1b9db681-a297-5aa9-e063-6394a90a80ea2025-06-25WarningsExact identifier
application number: M017
Hilook Numbing CreamLIDOCAINEGuangdong Aimu Biological Technology Co., Ltd1b9f1a4c-ca0b-d820-e063-6394a90a32392025-06-25WarningsExact identifier
application number: M017
Lidocaine Knee Pain Relief Gel-PatchLIDOCAINEGuangzhou Zhupuyou E-commerce Co., Ltd384c1ff8-80bd-86cb-e063-6394a90a2d652025-06-24WarningsExact identifier
application number: M017
Aroamas Cot Nicotine Transdermal Patches KitNICOTINE TRANSDERMAL PATCHESPCHEERY LLC38576022-9413-c9af-e063-6294a90afd462025-06-24WarningsExact identifier
application number: M017
NERVE REVERSE PAIN RELIEFMENTHOLPogue Medical Servicesda97bcc6-5aa8-48e2-a2c2-c937745bf6d32025-06-23WarningsExact identifier
application number: M017
Medterra Pain Relief Menthol Roll-OnMENTHOLRespect Manufacturing Corporation05a6067a-287a-52d4-e063-6394a90a2c4e2025-06-23WarningsExact identifier
application number: M017
Medterra Pain Relief 500mg Hemp Menthol CreamMENTHOLRespect Manufacturing Corporation06c4640a-ee42-5d1a-e063-6394a90ad2542025-06-23WarningsExact identifier
application number: M017
Medterra Pain Relief 1000mg Hemp Menthol CreamMENTHOLRespect Manufacturing Corporation06e944e8-71f6-9fe9-e063-6294a90a8c372025-06-23WarningsExact identifier
application number: M017
Procure gelMENTHOLTWIN MED, LLCe69c0b68-d408-9fd2-e053-2a95a90ac9342025-06-20WarningsExact identifier
application number: M017
A Health Itch Relief GelITCH RELIEF GELBionpharma, Inc.38040732-48c9-3533-e063-6394a90af10a2025-06-20WarningsExact identifier
application number: M017
SCHOELIF Numbing CreamNUMBING CREAMGuangzhou Qiexiran Cosmetics Co., Ltd.37eaabb7-884e-0bd5-e063-6294a90ae0632025-06-19WarningsExact identifier
application number: M017
Re-Lieved Lidocaine PatchLIDOCAINE PATCH 4%Transfer Technology37ee539c-df7e-511d-e063-6394a90a44692025-06-19WarningsExact identifier
application number: M017
Re-Lieved Lidocaine PatchLIDOCAINE PATCH 4%Transfer Technology37eef80a-556f-b090-e063-6294a90a151b2025-06-19WarningsExact identifier
application number: M017
Re-Lieved Lidocaine PatchLIDOCAINE PATCH 4%Transfer Technology37ef02d4-2ff5-cb23-e063-6294a90a68af2025-06-19WarningsExact identifier
application number: M017
Post-Treatment Repair CreamHYDROCORTISONEVi Medical Products Inc.ab8885a9-0778-28ff-e053-2995a90a2e122025-06-19WarningsExact identifier
application number: M017
MyDermLIDOCAINEInspec Solutions LLC.82d075d1-c92e-2097-e053-2991aa0ab1312025-06-18WarningsExact identifier
application number: M017
Walgreens Extra Small LidocaineLIDOCAINEWalgreen Co.dc838e47-d234-4ba5-9449-f645e99be9232025-06-18WarningsExact identifier
application number: M017
CLn Body MoisturizerCOLLOIDAL OAT MOISTURIZERTopMD Skin Care, Inc.2de3d68d-a540-d456-e063-6394a90a4b572025-06-18WarningsExact identifier
application number: M017
Aloe UP SPF 30 MineralZINC OXIDE, TITANIUM DIOXIDEAloe Care International, LLC35967b33-bdfb-ee3c-e063-6294a90a75f62025-06-18WarningsExact identifier
application number: M017
Aloe Up SPF 50 MineralZINC OXIDE, TITANIUM DIOXIDEAloe Care International, LLC35b9dcfa-05f3-3d7b-e063-6394a90a18f12025-06-18WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046313benzocaine 6 % / ethanol 60 % Medicated PadPSN364c9882-339e-fe22-e063-6294a90a37f42
1046313benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated PadSCD364c9882-339e-fe22-e063-6294a90a37f42
1046313benzocaine 6 % / ethanol 60 % Topical SwabSY364c9882-339e-fe22-e063-6294a90a37f42

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
72459-022-0172459002201.8 g in 1 PATCH (72459-022-01) 2025-06-02NoNoCurrent