FDA.reportPublic FDA data

NDC 61040-007 - First Aid Only First Aid/Burn

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
61040-007
Manufacturer
Acme United Corporation
Effective date
2023-10-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
First Aid Only First Aid/Burn - Acme United CorporationAcme United Corporation2023-10-09HUMAN OTC DRUG LABEL

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 100 of 233 · 4,643 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PUR-WASHWATERNiagara Pharmaceuticals Inc.e07a064b-f680-405c-bbcd-24fac430951e2025-11-24WarningsExact identifier
unii: 059QF0KO0R
ULINE EyewashEYEWASHNiagara Pharmaceuticals Inc.2d7f22d2-320b-6af1-e063-6294a90addc62025-11-24WarningsExact identifier
unii: 059QF0KO0R
Pur-WashEYEWASHNiagara Pharmaceuticals, Inc.0d43b1c1-2699-37f1-e054-00144ff88e882025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.777e1559-786f-8d54-e053-2991aa0aa98d2025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.7289103a-5cbf-42f4-8848-e827149a43ca2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Thermacare Heat Therapy Max Strength Lidocaine Pain Relief GelTHERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF GELClarion Brands LLC445db02a-c8e8-6ebb-e063-6294a90a43012025-11-24WarningsExact identifier
unii: V13007Z41A
Protex Balance antibacterial handBENZALKONIUM CHLORIDEColgate-Palmolive Companyd2514b67-303a-40f4-867b-9f41c0c8cba82025-11-24WarningsExact identifier
unii: F5UM2KM3W7
Rain Daily Hydration and Comfort For Dry EyesGLYCERINRain Eye Drops, LLC31d7c204-fb74-fb28-e063-6294a90ab3302025-11-23WarningsExact identifier
unii: PDC6A3C0OX
Lights SwabsticksISOPROPYL ALCOHOLLights Medical Manufacture Co., Ltd.4435a4e6-46ae-f49b-e063-6394a90a1d9e2025-11-22WarningsExact identifier
application number: M003
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEProPharma Distribution42df73b0-20ee-d1aa-e063-6294a90aa2752025-11-21Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
FloraMedis Hand SanitizerHAND SANITIZERSichuan Pengtai Qifan Technology Co., Ltd4415ca9f-10b1-88f7-e063-6294a90a2e092025-11-21WarningsExact identifier
application number: M003
unii: F5UM2KM3W7
DG 4x Medicated Tooth and Gum CreamBENZOCAINEDollar Generalb2c156f0-6d11-1eba-e053-2995a90a6db82025-11-21WarningsExact identifier
unii: F5UM2KM3W7
4x Medicated Toothache and Gum GelBENZOCAINECVSa7577d5f-69cf-3f32-e053-2995a90aaba52025-11-21WarningsExact identifier
unii: F5UM2KM3W7
Nighttime 4X Medicated CreamBENZOCAINERite Aid21645ed1-2dc0-223a-e063-6394a90ab0212025-11-21WarningsExact identifier
unii: F5UM2KM3W7
4x Medicated Gum CreamBENZOCAINEAlbertsonsb81a308c-9c30-0e3d-e053-2a95a90a15d22025-11-21WarningsExact identifier
unii: F5UM2KM3W7
pre fenseBENZALKONIUM CHLORIDEPrefense LLCfad70060-8bb6-4b06-a353-666132f64c262025-11-21WarningsExact identifier
unii: F5UM2KM3W7
pre fense unscentedBENZALKONIUM CHLORIDEPrefense LLCa59e9bbf-b60e-970a-e053-2a95a90aaa5e2025-11-21WarningsExact identifier
unii: F5UM2KM3W7
GelusilALUMINA, MAGNESIA, SIMETHICONEWellSpring Pharmaceutical Corporation92fbeec1-1562-40f3-9734-41f133d494f92025-11-20WarningsExact identifier
unii: 92RU3N3Y1O
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
unii: 059QF0KO0R
GERI-MOX ANTACID ANTIGASALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONEGeri-Care Pharmaceuticals, Corp03358bc7-8819-4a05-bc13-27fbf486bd262025-11-20WarningsExact identifier
unii: 92RU3N3Y1O

Reported adverse events (FAERS/openFDA)#

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