FDA.reportPublic FDA data

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#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Salicylic AcidACTIVE INGREDIENTO414PZ4LPZSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
Salicylic AcidACTIVE MOIETYO414PZ4LPZSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
aloe vera leafINACTIVE INGREDIENTZY81Z83H0XSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
ammonium lauryl sulfateINACTIVE INGREDIENTQ7AO2R1M0BSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
ammonium xylenesulfonateINACTIVE INGREDIENT4FZY6L6XCMSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
citric acid monohydrateINACTIVE INGREDIENT2968PHW8QPSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
DMDM hydantoinINACTIVE INGREDIENTBYR0546TOWSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
edetate sodiumINACTIVE INGREDIENTMP1J8420LUSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
hamamelis virginiana topINACTIVE INGREDIENTUDA30A2JJYSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
mentholINACTIVE INGREDIENTL7T10EIP3ASTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
PPG-5-ceteth-20INACTIVE INGREDIENT4AAN25P8P4STRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
sodium borateINACTIVE INGREDIENT91MBZ8H3QOSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]1
waterINACTIVE INGREDIENT059QF0KO0RSTRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC]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 78 of 217 · 4,327 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MENTHOL COUGH SUPPRESSANT ORAL ANESTHETIC Cough DropsMENTHOLXiamen Kang Zhongyuan Biotechnology Co., Ltd.29f2acaa-2cc8-a999-e063-6294a90a15ce2025-12-29WarningsExact identifier
unii: L7T10EIP3A
CVS cold and HotMENTHOL 16%CVSd1676df9-530f-1664-e053-2995a90a5b642025-12-29WarningsExact identifier
unii: L7T10EIP3A
Pain ReleaseMENTHOLNatures Formulae Health Products Ltd.781d3c8d-7b70-e973-e053-2991aa0aaa782025-12-29WarningsExact identifier
unii: L7T10EIP3A
Pain ReleaseMENTHOLNatures Formulae Health Products Ltd.781dfd66-f006-a2d7-e053-2991aa0a170c2025-12-29WarningsExact identifier
unii: L7T10EIP3A
FortifyMENTHOLNatures Formulae Health Products Ltd.781d53cf-b3dc-3e2b-e053-2a91aa0a7dcd2025-12-29WarningsExact identifier
unii: L7T10EIP3A
Pain ReleaseMENTHOLNatures Formulae Health Products Ltd.781d53cf-b3df-3e2b-e053-2a91aa0a7dcd2025-12-29WarningsExact identifier
unii: L7T10EIP3A
Salicylic AcidMEDICATED CALLUS REMOVERSFoodhold USA29e3caa0-4dc5-44d7-b7db-8bf45f6424ea2025-12-29WarningsExact identifier
unii: O414PZ4LPZ
Trauma LessMENTHOLNatures Formulae Health Products Ltd.781e94d5-1d34-7202-e053-2991aa0ae7682025-12-29WarningsExact identifier
unii: L7T10EIP3A
Blemish Spot TreatmentSALICYLIC ACIDSkin Script, LLC1bf92da8-35bf-5f32-e063-6294a90a71cf2025-12-29WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
Salicylic AcidMEDICATED CALLUS REMOVERSAmerisourceBergen Drug Corporation6aa867ee-4dd0-4308-9841-898d1ffe1edd2025-12-29WarningsExact identifier
unii: O414PZ4LPZ
Salicylic AcidMEDICATED CALLUS REMOVERSHarris Teeter, LLC0e649195-2e3b-48da-99e6-6f2c7fd686f22025-12-29WarningsExact identifier
unii: O414PZ4LPZ
Salicylic AcidMEDICATED CALLUS REMOVERSDiscount Drug Martf9ccb61c-e7cb-442c-aca9-f2ce6b4a4e432025-12-29WarningsExact identifier
unii: O414PZ4LPZ
Quality Choice Cold Therapy GelMENTHOLChain Drug Marketing Association, Inc.f9c659cd-e7fa-ac2d-e053-6294a90a25732025-12-29WarningsExact identifier
unii: L7T10EIP3A
Hot and Cold Medicated PatchMENTHOLHarris Teeter9debd4ef-c21b-41ae-afd1-58f47c51c99c2025-12-29WarningsExact identifier
unii: L7T10EIP3A
Pain Relief PatchesCAMPHOR, MENTHOL, METHYL SALICYLATEHarris Teeter3f5b4eee-49c4-408c-9af2-e7924c26ac632025-12-29WarningsExact identifier
unii: L7T10EIP3A
talc-free medicated bodyMENTHOLDavion, Inc27b9b4dc-4d4f-4e9d-b388-a7c6807a0e9b2025-12-29WarningsExact identifier
unii: L7T10EIP3A
H-E-B Medicated Corn Starch Foot PowderMENTHOLDavion, Inca6675e00-bc6b-4466-a283-4cece5f919702025-12-29WarningsExact identifier
unii: L7T10EIP3A
Maximum Strength Medicated Foot PowderMENTHOLDavion, Inc7b442d99-ac19-4f65-828d-954c5350ef5a2025-12-29WarningsExact identifier
unii: L7T10EIP3A
OCUFRESHWATEROptics Laboratory Inc.b8e477a9-66b9-496b-92fb-3d4bbd7b36b52025-12-29WarningsExact identifier
unii: 059QF0KO0R
HEB Medicated Cornstarch Body PowderMENTHOLDavion, Incdf1331fb-48df-4f21-8564-0468078fd12d2025-12-29WarningsExact identifier
unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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