FDA.reportPublic FDA data

NDC 12090-1041 - HORSEMANS DREAM FUNG-A-WAY

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
12090-1041
Package NDCs from labels
12090-1041-6
Manufacturer
SUMMIT INDUSTRIES | GDMI, INC
Effective date
2010-09-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
HORSEMANS DREAM FUNG-A-WAY - SUMMIT INDUSTRIES | GDMI, INCSUMMIT INDUSTRIES | GDMI, INC2010-09-17OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12090-1041-6HORSEMANS DREAM FUNG-A-WAY453.6 mL in 1 BOTTLESOLUTION453.61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12090-1041HORSEMANS DREAM FUNG-A-WAY (BENZALKONIUM CHLORIDE) SOLUTION [SUMMIT INDUSTRIES]11 package rows20100920_06bdf766-5a3b-4248-8a2b-e03b2c2bf5d4.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W7HORSEMANS DREAM FUNG-A-WAY (BENZALKONIUM CHLORIDE) SOLUTION [SUMMIT INDUSTRIES]1
BENZALKONIUMACTIVE MOIETY7N6JUD5X6YHORSEMANS DREAM FUNG-A-WAY (BENZALKONIUM CHLORIDE) SOLUTION [SUMMIT INDUSTRIES]1
ALLANTOININACTIVE INGREDIENT344S277G0ZHORSEMANS DREAM FUNG-A-WAY (BENZALKONIUM CHLORIDE) SOLUTION [SUMMIT INDUSTRIES]1
QUATERNIUM-15INACTIVE INGREDIENTE40U03LEM0HORSEMANS DREAM FUNG-A-WAY (BENZALKONIUM CHLORIDE) SOLUTION [SUMMIT INDUSTRIES]1
UREAINACTIVE INGREDIENT8W8T17847WHORSEMANS DREAM FUNG-A-WAY (BENZALKONIUM CHLORIDE) SOLUTION [SUMMIT INDUSTRIES]1
WATERINACTIVE INGREDIENT059QF0KO0RHORSEMANS DREAM FUNG-A-WAY (BENZALKONIUM CHLORIDE) SOLUTION [SUMMIT INDUSTRIES]1

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 65 of 72 · 1,438 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lightning X AntisepticBENZALKONIUM CHLORIDENantong Health & Beyond Hygienic Products Inc.0e6b10e7-6e84-6bfc-e063-6294a90a85372024-01-08WarningsExact identifier
unii: F5UM2KM3W7
F02 ANGR-FLXADELHEID AQUA, ARSENICUM ALBUM, BIG SAGEBRUSH, BOS TAURUS LIVER, GALLBLADDER, BRIZA MAXIMA, CALENDULA OFFICINALIS, CAYENNE, CHAMOMILE , CHICORY , GARLIC, ENGLISH HOLLY , EUROPEAN BEECH , FORKING LARKSPUR , GERMAN CHAMOMILE , IMPATIENS GLANDULIFERA , JUGLANS REGIA , LILIUM TIGRINUM, MORNING GLORY, MOUNTAIN DOGWOOD, NATRUM MURIATICUM, NUX VOMICA, PINUS SYLVESTRIS , REDWOOD, RUBBER RABBITBRUSH, SEPIA, TOLMIE STAR TULIP, VERBENA OFFICINALIS , VITIS VINIFERA , WATERMELON, WHITE WILLOW , YELLOW STAR THISTLEApex Energetics Inc.bc7c2bf3-8b0d-766f-e053-2a95a90ad34c2024-01-08WarningsExact identifier
unii: 059QF0KO0R
F09 LTGOADELHEID AQUA, AGRIMONY, MALUS SYLVESTRIS, ARSENICUM ALBUM, FILAREE, HEATHER, HORSE CHESTNUT, LACHESIS MUTUS, NASTURTIUM, RED HORSE CHESTNUT, SEPIA, SILICEA, STRAMONIUM, VERBENA OFFICINALISApex Energetics Inc.bd1e652f-b3a4-c5bd-e053-2995a90ae03f2024-01-08WarningsExact identifier
unii: 059QF0KO0R
Fendall 2000 Pure FlowPURIFIED WATERHoneywell Safety Products USA, Inc.b56ef662-fec2-4d94-e053-2995a90aba2b2024-01-06WarningsExact identifier
unii: 059QF0KO0R
OKeeffes Healthy FeetALLANTOIN, LIDOCAINEThe Gorilla Glue Company/O'Keeffe's Companyd73709db-3932-3c56-e053-2995a90a7d0a2024-01-01WarningsExact identifier
unii: 344S277G0Z
GLOBAL CARE GOLD ANTIBACTERIAL HANDBENZALKONIUM CHLORIDENINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.27ba0f30-e066-f240-e063-6394a90ae7cb2024-01-01WarningsExact identifier
unii: F5UM2KM3W7
Leader Eye WashPURIFIED WATERCardinal Health8d3ad11f-1945-f838-e053-2995a90a7aa52023-12-23WarningsExact identifier
unii: 059QF0KO0R
CVS MerthiolateBENZALKONIUM CHLORIDECVS Pharmacydd498ab1-8350-41aa-86fc-2db57005f3e22023-12-22WarningsExact identifier
unii: F5UM2KM3W7
MerthiolateBENZALKONIUM CHLORIDEPharma Nobis, LLCe42f727c-beaf-fe9d-e053-2995a90aafea2023-12-22WarningsExact identifier
unii: F5UM2KM3W7
GERMisept Antibacterial Hand Sanitizing WipesBENZALKONIUM CHLORIDEInnovent Incba4a04dc-7740-bd1b-e053-2995a90a089c2023-12-21WarningsExact identifier
unii: F5UM2KM3W7
RevitaDERM Wound CareBENZALKONIUM CHLORIDEBlaine Labs Inc.9254dada-4e32-43a0-892b-c488d68e23e72023-12-21WarningsExact identifier
unii: F5UM2KM3W7
Quality Choice MerthiolateBENZALKONIUM CHLORIDEChain Drug Market Association5b7303b9-b8c4-4e7c-876f-70ed764430552023-12-20WarningsExact identifier
unii: F5UM2KM3W7
Lite n Foamy Non-Alcohol Hand SanitizerLITE N FOAMY NON-ALCOHOL HAND SANITIZERSpartan Chemical Companyee8be683-f935-b32b-e053-2995a90aa51f2023-12-19WarningsExact identifier
unii: F5UM2KM3W7
Lite nFoamy E3 Hand SanitizerBENZALKONIUM CHLORIDESpartan Chemical Company2754e9bf-8c81-45b6-b243-993b9c4f99562023-12-19WarningsExact identifier
unii: F5UM2KM3W7
Calm and Heal Melting BalmALLANTOINThe Honest Company, Inc.b08a1bd6-986d-9520-e053-2995a90a865e2023-12-19WarningsExact identifier
unii: 344S277G0Z
Tincture MerthiolateBENZALKONIUM CHLORIDEDLC Laboratories, Inc4fec9119-fbbf-4fc7-9122-c6300cac87312023-12-18WarningsExact identifier
unii: F5UM2KM3W7
HUMCO MerthiolateBENZALKONIUM CHLORIDEHumco Holding Group, Inc.864063a5-c6cc-4657-9cd6-51af4673bf982023-12-15WarningsExact identifier
unii: F5UM2KM3W7
TaeTu AftercareBENZALKONIUM CHLORIDETaetu LLCdec15a4d-1a33-a78a-e053-2995a90a69fe2023-12-14WarningsExact identifier
unii: F5UM2KM3W7
Antibacterial Wet WipesBENZALKONIUM CHLORIDEHangZhou YangYi Daily Cosmetics Technology Co., Ltd.85d3914d-dbb8-5036-e053-2a91aa0a7cd42023-12-13WarningsExact identifier
unii: F5UM2KM3W7
Eye WashWATERJiangxi Zhenmei Biological Technology Co.,Ltdc68795b8-bf68-0d01-e053-2a95a90abebb2023-12-04WarningsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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