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 154 of 214 · 4,269 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Rite Aid Hot and Cold Roll OnMENTHOL 16%Rite Aidfc4b2635-280b-267f-e053-6294a90a5e222024-12-15WarningsExact identifier
unii: L7T10EIP3A
Rite Aid Pain RelievingBENZOCAINE 20%, MENTHOL 0.5%Rite Aide2c09e85-be0a-4e6d-e053-2995a90ad7562024-12-15WarningsExact identifier
unii: L7T10EIP3A
Rite Aid Cooling Pain ReliefMENTHOL 10.5%Rite Aide2225259-70ec-52de-e053-2a95a90a73f82024-12-15WarningsExact identifier
unii: L7T10EIP3A
Dermisa Acne TreatmentBENZOYL PEROXIDEMontani Cosmetics Incd61a6354-8194-da19-e053-2995a90a7e222024-12-15WarningsExact identifier
application number: M006
QC Cool and Heat Roll-OnMENTHOL 16%Chain Drug Marketing Association Incd35e9dfa-8a28-fdb3-e053-2995a90abc522024-12-15WarningsExact identifier
unii: L7T10EIP3A
Meijer Cold and Hot Pain RelievingMENTHOL 16%Meijerbec62df3-06c9-a115-e053-2995a90a42672024-12-15WarningsExact identifier
unii: L7T10EIP3A
Tommie Copper Pain ReliefMENTHOL 16%Tommie Copper, Inc.b4dfa5fa-2d61-db1e-e053-2a95a90a7ac82024-12-15WarningsExact identifier
unii: L7T10EIP3A
Pain Relief Liquid RollerCAMPHOR 3.5%, MENTHOL 3.5%Tommie Copper, Inc.c9f0447e-de43-16a5-e053-2995a90a05c12024-12-15WarningsExact identifier
unii: L7T10EIP3A
Tommie Copper Pain Relief RollerCAMPHOR 3.5%, MENTHOL 3.5%Tommie Copper, Inc.b6c3d6eb-b485-33b8-e053-2a95a90a41e12024-12-15WarningsExact identifier
unii: L7T10EIP3A
Tommie Copper Pain Relief RollerCAMPHOR 3.5%, MENTHOL 3.5%Tommie Copper, Inc.b4cd4fed-e8c8-db85-e053-2995a90a708b2024-12-15WarningsExact identifier
unii: L7T10EIP3A
Copperlife Pain Relief LiquidMENTHOL 16%Tommie Copper, Inc.c93a0139-953b-5523-e053-2a95a90a0b2d2024-12-15WarningsExact identifier
unii: L7T10EIP3A
Mentholatum OriginalCAMPHOR, MENTHOLThe Mentholatum Company19e4b812-67c6-49fd-833a-b432100363f52024-12-13WarningsExact identifier
unii: L7T10EIP3A
OXY ADVANCED CARE 3 in 1 RETEXTURIZING CLEANSING PADSSALICYLIC ACIDThe Mentholatum Companyc36f7012-6fc7-4141-8492-6a20d3cf48682024-12-13WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
Cold and Hot MedicatedMENTHOLThe Mentholatum Company85bf425d-59d7-4462-ba46-2921454600992024-12-13WarningsExact identifier
unii: L7T10EIP3A
OXY ADVANCED CARE MAXIMUM STRENGTH 3-in-1 ACNE PADSSALICYLIC ACIDThe Mentholatum Company99874117-b1f5-48bf-a1b1-3a2af9d9ae272024-12-13WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
OXY Advanced Care Sensitive Skin Acne CleanserBENZOYL PEROXIDEThe Mentholatum Company4967f854-d1e4-4fb6-84c7-1293f5f906302024-12-13WarningsExact identifier
application number: M006
OXY Advanced Care Soothing Cream Acne CleanserBENZOYL PEROXIDEThe Mentholatum Company4171b8a9-7ebf-4c02-a086-87038b6c68c42024-12-13WarningsExact identifier
application number: M006
Oxy Advanced Care Rapid Spot TreatmentBENZOYL PEROXIDEThe Mentholatum Companye613e8a6-ffed-49bc-bdc0-87606c51ffa32024-12-13WarningsExact identifier
application number: M006
OXY Advanced Care Soothing Cream Acne CleanserBENZOYL PEROXIDEThe Mentholatum Company76fddd7e-8323-4046-8c90-2edafc3e09372024-12-13WarningsExact identifier
application number: M006
pHisoderm Clear Confidence Face ScrubSALICYLIC ACIDThe Mentholatum Companyb3213f88-9496-4c89-ab1b-225bd81891c22024-12-13WarningsExact identifier
application number: M006
unii: O414PZ4LPZ

Reported adverse events (FAERS/openFDA)#

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