NDC 69574-005-04 - NOVUM APR

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
69574-005
Requested NDC
69574-005-04
Package NDCs from labels
69574-005-04, 69574-005-05
Manufacturer
NOVUM SOLUTIONS INC | Bio-Medical & Pharmaceutical Manufacturing Corporation
Effective date
2025-04-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
NOVUM APR - NOVUM SOLUTIONS INC | Bio-Medical & Pharmaceutical Manufacturing CorporationNOVUM SOLUTIONS INC | Bio-Medical & Pharmaceutical Manufacturing Corporation2025-04-07HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69574-005-04NOVUMAPR118.3 mL in 1 BOTTLE, SPRAYSPRAY118.37
69574-005-05NOVUMAPR1 in 1 BOXSPRAY17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69574-005NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC]7Current NDC, Legacy NDC, 2 package rows20250409_1b869a1f-5787-4d03-a546-43a8217b2b2c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MENTHOLACTIVE INGREDIENTL7T10EIP3ANOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC]3
MENTHOLACTIVE MOIETYL7T10EIP3ANOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC]3
EUCALYPTUS OILINACTIVE INGREDIENT2R04ONI662NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC]3
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M416302NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC]3
METHYL SALICYLATEINACTIVE INGREDIENTLAV5U5022YNOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC]3
SPEARMINT OILINACTIVE INGREDIENTC3M81465G5NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC]3
WATERINACTIVE INGREDIENT059QF0KO0RNOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC]3

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 48 of 241 · 4,811 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lightning Pain ReliefMENTHOLClinical Resolution Laboratory, Inc.80af21f5-dba8-42b0-8a65-ac5a94d83ca82026-03-02WarningsExact identifier
application number: M017
unii: L7T10EIP3A
Isopropyl alcohol 91 percentISOPROPYL ALCOHOLTARGET Corporationc49f46c5-f9b2-4045-a31d-63cb222102332026-03-02WarningsExact identifier
unii: ND2M416302
Isopropyl alcohol 91 percentISOPROPYL ALCOHOLSam's West, Inca9d6778a-e5ad-4e02-9142-4a932540eda72026-03-02WarningsExact identifier
unii: ND2M416302
Icy Hot Lidocaine No-MessLIDOCAINE HYDROCHLORIDEChattem, Inc.347f9a18-8ab6-47d3-9610-5b4e9ca5d53a2026-03-02WarningsExact identifier
application number: M017
Gold Bond Maximum Strength Foot Pain ReliefLIDOCAINE HYDROCHLORIDEGold Bond Co LLC8e469076-2f5a-4de8-8d13-a38c072b9af82026-03-01WarningsExact identifier
application number: M017
HealthWise Pain Relief LidocaineLIDOCAINE HYDROCHLORIDEVeridian Healthcare48ecbab9-13e0-d0fa-e063-6294a90a6ff22026-02-28WarningsExact identifier
application number: M017
NUMBING CREAMSLIDOCAINEYongchun Lihui Trading Co., Ltd.3b5e1a74-5946-4f1f-e063-6394a90a404b2026-02-27WarningsExact identifier
application number: M017
Pain Relieving GelLIDOCAINE HYDROCHLORIDEChain Drug Marketing Associationb55b7253-2fd2-45cc-b94c-e92395ab0d2b2026-02-27Warnings, Adverse reactionsExact identifier
application number: M017
Antiseptic MouthrinseEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLChain Drug Marketing Association27ff8499-63e0-49ad-a4dd-dde6da584f932026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
Antiseptic Mouth RinseEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLChain Drug Marketing Association1c4b22aa-4f2b-8f30-e063-6394a90a6ed52026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
Antiseptic MouthrinseEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLChain Drug Marketing Associationbd8a4b8b-cd59-4d0d-8ceb-40bba777e61b2026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
Mouth RinseEUCALYPTOL, MENTHOL, METHYLSALICYLATE, THYMOLThe Kroger Co.d97cdb55-c6bc-4138-ad1d-c7124d7f5cec2026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
Chest RubCAMPHOR, EUCALYPTUS OIL, MENTHOLThe Kroger Co.116146db-719f-4c48-8a8a-1120ea62b0d52026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: 2R04ONI662
AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLThe Kroger Co.e4844ad3-6073-4c2c-9029-5c4f4ea024e82026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
Tartar control plusEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLThe Kroger Co.0407d06e-a8d4-4522-8213-3a7a0c5e336e2026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
MEDISTIK PROFESSIONAL DUAL ACTIONMENTHOL, METHYL SALICYLATE, EUCALUPTUSNatureteq Inc.99c7f08a-ab14-4371-9147-189f75cb66332026-02-27WarningsExact identifier
application number: M017
unii: L7T10EIP3A
unii: LAV5U5022Y
Mouth RinseEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLThe Kroger Co.f6ccdce2-ae3c-44f7-803d-5a135a7a7e8e2026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
Antiseptic MouthrinseEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLWalmart Inc.a8daefba-b985-4ef9-b900-e5647324662e2026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
AntisepticEUCALYPTOL, MENTHOL, METYL SALICYLATE, THYMOLWalmart Inc.404dfa0f-8ac1-463a-9e10-fc87f70697952026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLWalmart Inc.d2515c9c-79b4-4874-be6e-fe8312477fc82026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y

Reported adverse events (FAERS/openFDA)#

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