NDC 10157-1007-01 - Stridex Sensitive

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
10157-1007
Requested NDC
10157-1007-01
Package NDCs from labels
10157-1007-1, 10157-1007-2, 10157-1007-3, 10157-1007-4, 10157-1007-01
Manufacturer
Blistex Inc
Effective date
2024-12-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Stridex Sensitive - Blistex IncBlistex Inc2024-12-12HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10157-1007-1Stridex Sensitive1 in 1 CARTONLIQUID13
10157-1007-1Stridex Sensitive55 in 1 JARLIQUID553
10157-1007-2Stridex Sensitive1 in 1 CARTONLIQUID13
10157-1007-2Stridex Sensitive70 in 1 JARLIQUID703
10157-1007-3Stridex Sensitive90 in 1 JARLIQUID903
10157-1007-3Stridex Sensitive1 in 1 CARTONLIQUID13
10157-1007-4Stridex Sensitive1 in 1 CARTONLIQUID13
10157-1007-4Stridex Sensitive110 in 1 JARLIQUID1103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10157-1007STRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]3Current NDC, Legacy NDC, 8 package rows20241215_843d3424-bd6c-44aa-976b-63c9da15014e.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10157-1007-1EA - Each10157-1007330a1a5d-859e-45d2-ba0a-b4b56c6e092412016-02-04
10157-1007-2EA - Each10157-1007c865aa9b-a970-4f43-a08c-e9186338f98912016-02-04

DailyMed Socrata Ingredients#

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 152 of 214 · 4,269 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dollar General Cold-Hot Medicated PatchesMENTHOLDOLGENCORP, LLCc6e0388b-af9e-4e51-8f94-6788185c31a02024-12-18WarningsExact identifier
unii: L7T10EIP3A
TheraCare Medicated Chest RubCAMPHOR, MENTHOL, EUCALYPTUS OILVeridian Healthcaref7801843-f96c-710e-e053-6294a90a50862024-12-18WarningsExact identifier
unii: L7T10EIP3A
TheraCare Medicated Pain Relief PatchesCAMPHOR, MENTHOL, METHYL SALICYLATEVeridian Healthcaref6f3c9c0-d6e3-75a3-e053-6294a90a19652024-12-18WarningsExact identifier
unii: L7T10EIP3A
Good Sense Hot and Cold Medicated PatchMENTHOLGOOD SENSE1b16c3e5-a29f-4043-94e6-0a0e0ea3d93e2024-12-18WarningsExact identifier
unii: L7T10EIP3A
ChestrubCAMPHOR MENTHOL EUCALYPTUS OILDelta Brands Inc8e6f731f-c16a-41b2-9786-0cab588cfc8e2024-12-17WarningsExact identifier
unii: L7T10EIP3A
OXY 3 in 1 Acne PadsSALICYLIC ACIDThe Mentholatum Company5b1c8f11-3b5b-4c26-b4c1-0770d1dd823a2024-12-17WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
Ultra Strength Muscle RubCAMPHOR, MENTHOL, METHYL SALICYLATEThe Mentholatum Company32b64985-0e2f-49ee-9840-946d7279fee72024-12-17WarningsExact identifier
unii: L7T10EIP3A
Mentholatum Nighttime Vaporizing RubCAMPHOR, EUCALYPTUS OIL, MENTHOLThe Mentholatum Company5539ae74-9723-480d-b35f-0a6644bf54ad2024-12-17WarningsExact identifier
unii: L7T10EIP3A
Phisoderm Clear Confidence Spot TreatmentBENZOYL PEROXIDEThe Mentholatum Company2a51c80a-27e8-44d3-b06f-b2a9081c57962024-12-17WarningsExact identifier
application number: M006
Mentholatum No Mess Vaporizing RubCAMPHOR, EUCALYPTUS OIL, MENTHOLThe Mentholatum Companyf4675bc1-01cc-4a33-a3bf-bfc99230fe322024-12-17WarningsExact identifier
unii: L7T10EIP3A
CVS Health Cold and Hot Pain Relieving Extra StrengthMENTHOL, METHYL SALICYLATECVS Pharmacy1ca1a631-cb2c-46cd-bd41-05469b08d2082024-12-17WarningsExact identifier
unii: L7T10EIP3A
Mentholatum Pain RelievingMENTHOL, METHYL SALICYLATEThe Mentholatum Company0056b952-9870-485a-9f35-f985472875a92024-12-17WarningsExact identifier
unii: L7T10EIP3A
Oxy 10 VanishingBENZOYL PEROXIDEThe Mentholatum Companyd499b69a-25aa-4e3d-a07e-a774bc0d65f12024-12-17WarningsExact identifier
application number: M006
OXY Volcanic Clay Acne WashSALICYLIC ACIDThe Mentholatum Companyeb2a0e0b-2ed5-4c14-8607-0b61ca48c4952024-12-17WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
OXY Volcanic Ash Acne Face WashSALICYLIC ACIDThe Mentholatum Company6d768d3d-c1df-4a85-9c76-7f7a2ec90b2d2024-12-17WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
Oxy 10 TintedBENZOYL PEROXIDEThe Mentholatum Company0ceee85d-dc8c-49b3-9b44-8fe60022c2432024-12-17WarningsExact identifier
application number: M006
Oxy 5 VanishingBENZOYL PEROXIDEThe Mentholatum Companyc4aa0fff-6e4a-47a8-9adc-ac2426f8292e2024-12-17WarningsExact identifier
application number: M006
Oxy 5 TintedBENZOYL PEROXIDEThe Mentholatum Company94c863f0-711a-4807-ba1f-a56c7e3f86702024-12-17WarningsExact identifier
application number: M006
Phisoderm Anti Blemish Body WashSALICYLIC ACIDThe Mentholatum Companybba14225-2970-4678-b5a1-78ed94c389d92024-12-17WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
Phisoderm Anti-Blemish Gel CleanserSALICYLIC ACIDThe Mentholatum Company9fd851bf-1113-488b-ad16-1a3ce52a87d52024-12-17WarningsExact identifier
application number: M006
unii: O414PZ4LPZ

Reported adverse events (FAERS/openFDA)#

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