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 168 of 214 · 4,269 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Walgreen Cool n Heat Maximum Strength Pain RelievingMENTHOL, UNSPECIFIED FORMWalgreen Companyd5c79476-dde8-4a85-8878-bc2ac3a3d70b2024-11-04WarningsExact identifier
unii: L7T10EIP3A
Walgreens Dandruff Itchy Dry Scalp Defense Plus Vitamins and Botanicals Anti-dandruffSALICYLIC ACIDWalgreen Company2776d45c-6597-4c13-81e6-29d9248e9e562024-11-01WarningsExact identifier
unii: O414PZ4LPZ
SkinMedica Acne Clarifying TreatmentSALICYLIC ACIDAllergan, Inc.664d4733-e72d-410a-8ed0-a159d9dfa2362024-11-01WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
Walgreens Nerve Pain Relieving Topical AnalgesicLIDOCAINE HYDROCHLORIDE AND MENTHOL, UNSPECIFIED FORMWalgreen Company83849eca-e02f-4b43-b3a7-b25e987e08a82024-10-31WarningsExact identifier
unii: L7T10EIP3A
Walgreens Acne Control Cleanser Acne MedicationBENZOYL PEROXIDEWalgreen Companyf33e4204-fed9-4f14-a00f-c81b1910254b2024-10-31WarningsExact identifier
application number: M006
Walgreens Acne Foaming Wash Acne MedicationBENZOYL PEROXIDEWalgreen Companyf34affe9-d470-48a5-b0d1-d62b9c44b3f22024-10-31WarningsExact identifier
application number: M006
ARCTIC RELIEFMENTHOL, UNSPECIFIED FORMSTRATUS PHARMACEUTICALS INCd27fbc17-46b7-4d52-ba29-c99b6c63144a2024-10-31WarningsExact identifier
unii: L7T10EIP3A
Vital Immune BoosterAPIS MELLIFICA, BORAX, CARDUUS MARIANUS, CISTUS CANADENSIS, ECHINACEA (ANGUSTIFOLIA), GALIUM APARINE, HEPAR SUIS, HEPAR SULPHURIS CALCAREUM, HGH, HYPOPHYSIS SUIS, NITRICUM ACIDUM, PHYTOLACCA DECANDRA, SULPHUR IODATUM, THUJA OCCIDENTALIS, THYMUS SUISLiddell Laboratories, Inc.2950dd59-0633-4c62-9aaa-a808e2dbec652024-10-31WarningsExact identifier
unii: 91MBZ8H3QO
Pain Relief Gel-PatchLIDOCAINE, MENTHOLR & Y Group, LLCfe0478d8-2f06-cd56-e053-6294a90a58e52024-10-30WarningsExact identifier
unii: L7T10EIP3A
JOINT-RITIS PAIN RELIEVING ROLL-ONMENTHOLLifeline Naturals of America, Inc.ec5d99c4-6bba-45d1-84e0-12fb7cb314952024-10-30WarningsExact identifier
unii: L7T10EIP3A
Walgreens Pain Relieving AnalgesicCAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATEWalgreen Company3215a676-104c-43c3-aa36-b30d5b67799a2024-10-30WarningsExact identifier
unii: L7T10EIP3A
Clearing Skin WashSALICYLIC ACIDDermalogica, LLC.5cd31221-d6b4-47b9-99fd-fdfc2e1b6fdf2024-10-30WarningsExact identifier
application number: M006
unii: O414PZ4LPZ
Ultra-Strength Pain Relief AnalgesicCAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORMTARGET CORPORATION159c5a84-bf68-41dd-a2d3-bc24020372442024-10-30WarningsExact identifier
unii: L7T10EIP3A
Walgreens Acne Foaming Cleanser Acne TreatmentBENZOYL PEROXIDEWalgreen Company5b6fab38-4a9e-4c5c-967e-e3a0ff03b6062024-10-30WarningsExact identifier
application number: M006
DG Health Cold n Hot Pain Relieving Topical AnalgesicMENTHOL, UNSPECIFIED FORMDolgencorp Inc8fe13b85-ab74-42f8-a664-d3d2959921ac2024-10-30WarningsExact identifier
unii: L7T10EIP3A
Granulotion MedicatedMENTHOL, ZINC OXIDEGL HEALTH, INC.01701780-b160-415b-b34d-3622371794752024-10-29WarningsExact identifier
unii: L7T10EIP3A
HealthWise Medicated Chest RubCAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOLVeridian Healthcare25a19d3e-37b3-50d5-e063-6394a90a97d12024-10-29WarningsExact identifier
unii: L7T10EIP3A
Menthol Cough DropsMENTHOLBOSTON NUTRACEUTICAL PRODUCTION, S.Le82dac83-2910-44dc-e053-2995a90a38e12024-10-29WarningsExact identifier
unii: L7T10EIP3A
TheraCare Medicated Chest RubCAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOLVeridian Healthcared6e789c7-a55a-dc9a-e053-2a95a90a2bdb2024-10-29WarningsExact identifier
unii: L7T10EIP3A
ZO Skin Health Acne Control Benzoyl PeroxideBENZOYL PEROXIDEZO Skin Health, Inc.252b2352-a457-4009-a62b-0ec98f018b2e2024-10-28WarningsExact identifier
application number: M006

Reported adverse events (FAERS/openFDA)#

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