Home NDC 82749-010 Sting Relief Swab
Product NDC 82749-010
11-digit product format 827490010
Labeler code 82749
Product ID 82749-010_2b202e3c-e544-95eb-e063-6394a90a15fe
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form SWAB
Route TOPICAL
Labeler Epic Medical Supply Corp
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-10-29
Substance MENTHOL, UNSPECIFIED FORM; BENZOCAINE
Active strength .006; .12 g/.6mL; g/.6mL
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 Sting Relief Swab
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM .006 g/.6mL BENZOCAINE .12 g/.6mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup U3RSY48JW5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1037117 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82749-010-01 Sting Relief Swab 6 mL in 1 CARTON SWAB 6 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82749-010 STING RELIEF SWAB (BENZOCAINE) SWAB [EPIC MEDICAL SUPPLY CORP] 2 Current NDC, 1 package rows 20250109_259fbfe4-d67c-ea1e-e063-6294a90a0fb0.zip
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 133 of 151 · 3,010 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Dermachange Cold Therapy MENTHOL Private Label Beauty and Wellness 12ef7dd8-3da3-9c87-e063-6394a90ac924 2024-03-05 Warnings Exact identifier application number: M017 Dermachange Arthritis Relief TROLAMIN SALICYLATE Private Beauty Label and Wellness 12dbfa50-1b97-f988-e063-6394a90a662c 2024-03-04 Warnings Exact identifier application number: M017 Analgesic MENTHOL Safetec of America, Inc. b0f4010c-995f-40e1-aa40-92760e697a61 2024-03-02 Warnings Exact identifier application number: M017 Icy Hot Advanced Relief CAMPHOR AND MENTHOL Chattem, Inc. 9979ff36-415b-44e4-bb10-6bf682cd00f9 2024-03-01 Warnings Exact identifier application number: M017 Amish Origins Pain Relieving Menthol 8% MENTHOL Amish Origins Management, LLC 5051b650-18a4-481e-a8d7-d41d4ae51efd 2024-02-29 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE TRIFECTA PHARMACEUTICALS USA LLC 2999fecb-cb15-4023-ade4-ab5822b094d5 2024-02-29 Warnings Exact identifier application number: M017 Amish Origins Pain Relieving Menthol 8 MENTHOL Amish Origins Management, LLC aaad56d5-6737-4edc-af0e-8e207695c0ec 2024-02-29 Warnings Exact identifier application number: M017 Amish Origins Pain Relieving Menthol 8% MENTHOL Amish Origins Management, LLC b120404f-5a07-4182-bb50-d943418622da 2024-02-29 Warnings Exact identifier application number: M017 Amish Origins Topical Analgesic Camphor 2% CAMPHOR (SYNTHETIC) Amish Origins Management, LLC 437491ca-60ff-4508-b408-f97e7152f638 2024-02-29 Warnings Exact identifier application number: M017 Amish Origins Topical Analgesic Camphor 2% CAMPHOR (SYNTHETIC) Amish Origins Management, LLC ffe15aed-ea90-4db8-aace-d691a81c05ae 2024-02-29 Warnings Exact identifier application number: M017 LidoPro Patch LIDOCAINE, MENTHOL, AND METHYL SALICYLATE Advanced Rx Pharmacy of Tennessee, LLC 128d0ba9-bc9d-af16-e063-6394a90af5ef 2024-02-29 Warnings Exact identifier application number: M017 Leader Roll-On Cooling Pain Relief Topical Analgesic MENTHOL, UNSPECIFIED FORM Cardinal Health, 110 dba LEADER e86cba40-6b10-454d-98b3-6b547456eaad 2024-02-29 Warnings Exact identifier application number: M017 Maximum Strength Scalp Itch Relief Anti-itch HYDROCORTISONE Rite Aid 55569563-fc38-4f97-8e74-9f96e3173384 2024-02-28 Warnings Exact identifier application number: M017 Walgreens Eczema Relief HYDROCORTISONE ACETATE Walgreen Co. 4a65a1bf-aa24-4452-9ec3-a28c8bf0e47c 2024-02-28 Warnings Exact identifier application number: M017 meijer Cold Therapy Pain Relieving analgesic MENTHOL, UNSPECIFIED FORM Meijer Distribution, Inc fb163112-d84d-418d-a410-3214c0ee4b5a 2024-02-28 Warnings Exact identifier application number: M017 SunBurnt PLUS LIDOCAINE HYDROCHLORIDE Quest Products, LLC. 12128c75-015d-8a72-e063-6394a90ae00a 2024-02-23 Warnings Exact identifier application number: M017 Kroger Analgesic Analgesic LIDOCAINE HYDROCHLORIDE THE KROGER CO e6c5ead3-87d0-48ed-a4dc-86cf89ebb285 2024-02-22 Warnings Exact identifier application number: M017 Rugby Pain Relieving Analgesic MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE Bryant Ranch Prepack fcf48536-224e-4a3d-9124-770031823972 2024-02-22 Warnings Exact identifier application number: M017 meijer ROLL-ON Cold Therapy Pain Relieving Topical analgesic MENTHOL, UNSPECIFIED FORM Meijer Distribution, Inc 8bc3956b-b82d-4ed3-8bc3-db0078466bbc 2024-02-22 Warnings Exact identifier application number: M017 Promescent Delay Wipes BENZOCAINE Absorption f0a5b6be-acc5-473c-9054-b9534e769db1 2024-02-20 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 82749-010-01 82749001001 6 mL in 1 CARTON (82749-010-01) 6 ml 2024-10-29 No No Current