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 134 of 214 · 4,277 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Neutrogena Stubborn Body Acne TreatmentSALICYLIC ACIDKenvue Brands LLCdd1436c0-aa9e-259c-e053-2a95a90a0b4c2025-04-08WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
OARS AND ALPS MUSCLE RECOVERY BALMMENTHOL, METHYL SALICYLATECosco International, Inc8745802f-018d-4cf8-bbf3-3b04c8f545382025-04-08WarningsExact identifier
unii: L7T10EIP3A
TreeActiv Cystic Acne Spot TreatmentSULFURLeiluna LLCd1b81650-ccc4-49ed-9378-726b3a3a04c72025-04-08WarningsExact identifier
application number: M006
NOVUM APRMENTHOLNOVUM SOLUTIONS INC1b869a1f-5787-4d03-a546-43a8217b2b2c2025-04-07WarningsExact identifier
unii: L7T10EIP3A
MAG 5 PT ROLL-ON PAIN RELIEF COOLINGMENTHOLRENU LABORATORIES, LLC31e4fa2c-3a98-d618-e063-6394a90aec1c2025-04-07WarningsExact identifier
unii: L7T10EIP3A
RockSauce FIERY HOT PAIN RELIEFMETHYL SALICYLATE, MENTHOL, CAPSAICINImplus Footcare, LLCcc7cbf4a-8274-e463-e053-2995a90a51e02025-04-07WarningsExact identifier
unii: L7T10EIP3A
RockSauce FIERY HOT PAIN RELIEFMETHYL SALICYLATE, MENTHOL, CAPSAICINImplus Footcare, LLCbdee018a-2c3c-3116-e053-2a95a90ac8d82025-04-07WarningsExact identifier
unii: L7T10EIP3A
RockSauce FIERY HOT PAIN RELIEFMETHYL SALICYLATE, MENTHOL, CAPSAICINImplus Footcare, LLCbdee2b65-2759-0e62-e053-2a95a90a03782025-04-07WarningsExact identifier
unii: L7T10EIP3A
RockSauce ICY COLD PAIN RELIEFMENTHOLImplus Footcare, LLCbdc7c7f3-ac98-8fe9-e053-2a95a90a26632025-04-07WarningsExact identifier
unii: L7T10EIP3A
RockSauce ICY COLD PAIN RELIEFMENTHOLImplus Footcare, LLCbd4fdff1-9174-31c2-e053-2a95a90a749f2025-04-07WarningsExact identifier
unii: L7T10EIP3A
CBD Clinic Pain Relief - Level 5MENTHOL, CAMPHORABACUS HEALTH PRODUCTS, INC.f0ebc1c6-93fb-efd6-e053-2995a90a25bb2025-04-07WarningsExact identifier
unii: L7T10EIP3A
CBD Clinic Pain Relief - Level 4MENTHOL, CAMPHORABACUS HEALTH PRODUCTS, INC.f0e9ac7c-a840-2e05-e053-2a95a90a33f12025-04-07WarningsExact identifier
unii: L7T10EIP3A
CBDMEDIC Active Sport Pain ReliefCAMPHOR AND MENTHOLABACUS HEALTH PRODUCTS, INC.f0ec5f47-2f8e-0558-e053-2a95a90aa7ca2025-04-07WarningsExact identifier
unii: L7T10EIP3A
MouthwashMENTHOL, METHYL SALICYLATE, THYMOLOrazen Inc873c43df-1d46-359b-e053-2a91aa0a43192025-04-07WarningsExact identifier
unii: L7T10EIP3A
LEAHUE MADHUCA TONICSALICYLIC ACIDBio-interchange Co.31ee4645-0f64-f7a0-e063-6394a90a17362025-04-04WarningsExact identifier
unii: O414PZ4LPZ
LEAHUE MADHUCASALICYLIC ACIDBio-interchange Co.81470dfe-f063-9d16-e053-2a91aa0a18292025-04-04WarningsExact identifier
unii: O414PZ4LPZ
AHA BHA Blemish Control and Exfoliating SerumSALICYLIC ACID SERUMBanuskin, Inc.31e47495-a9fa-a9e8-e063-6294a90a6b672025-04-03WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
Sulfur Spot TreatmentSULFUR ACNE TREATMENTBanuskin, Inc.31e527e0-ce37-e920-e063-6394a90ac8272025-04-03WarningsExact identifier
application number: M006
Hot Cold Medicated PatchesHOT COLD MEDICATED PATCHESHenan Enokon Medical Instrument Co., Ltd.159266a8-94fa-e2ff-e063-6394a90a9a772025-04-02WarningsExact identifier
unii: L7T10EIP3A
Pain Relief PatchPAIN RELIEF PATCHHenan Enokon Medical Instrument Co., Ltd.1592d29d-e275-a44d-e063-6294a90ab17d2025-04-02WarningsExact identifier
unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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