FDA.reportPublic FDA data

SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF

Product NDC
50090-6172
11-digit product format
500906172
Labeler code
50090
Product ID
50090-6172_8ccae7c4-e443-4cec-a31d-764334293b65
Type
HUMAN OTC DRUG
Nonproprietary name
polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride
Dosage form
OINTMENT
Route
TOPICAL
Labeler
A-S Medication Solutions
Application
M004
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-03-31
Marketing end
2027-08-31
Substance
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Active strength
500; 3.5; 10000; 10 [iU]/g; mg/g; [iU]/g; mg/g
Pharmacologic classes
Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Decreased Cell Wall Synthesis & Repair [PE], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
NDC exclude flag
No
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BACITRACIN ZINC500 [iU]/g
NEOMYCIN SULFATE3.5 mg/g
POLYMYXIN B SULFATE10000 [iU]/g
PRAMOXINE HYDROCHLORIDE10 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii89Y4M234ES, 057Y626693, 19371312D4, 88AYB867L5
Rxcui1359350

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
99e684e6-f435-feb8-d2bb-3a546f1cb768Product name220161117
25340b3b-3e4c-4ff8-abf6-3e62ec46bd0cProduct name120160603
2d352c73-a357-4193-a4de-dfdf9a2ac8e4Product name120150819
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
b6082387-f592-1148-0844-bd068fd213fbProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-6172-0SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF36 in 1 CASEOINTMENT362
50090-6172-0SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF28.4 g in 1 TUBEOINTMENT28.42

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-6172-0GM - Gram50090-6172d5e12f54-5a8b-42ae-8fb8-460948ce543912024-12-10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-6172SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF (POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE) OINTMENT [A-S MEDICATION SOLUTIONS]2Current NDC, 2 package rows20241025_01131ba6-6d5b-4710-bec3-ba1769c08c79.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1359350bacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine HCl 10 MG in GM Topical OintmentPSN01131ba6-6d5b-4710-bec3-ba1769c08c792
1359350bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 10 UNT/MG / pramoxine hydrochloride 0.01 MG/MG Topical OintmentSCD01131ba6-6d5b-4710-bec3-ba1769c08c792
1359350bacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine HCl 10 MG per GM Topical OintmentSY01131ba6-6d5b-4710-bec3-ba1769c08c792

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-6172-05009061720036 TUBE in 1 CASE (50090-6172-0) / 28.4 g in 1 TUBE36 tube2022-10-142027-08-31NoNoHistorical