STRIDEX

Manufacturer
Blistex inc
Effective date
2009-11-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:23:12

Label at a glance#

ProductSTRIDEX Naturally Clear
Active ingredientSALICYLIC ACID
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

 SALICYLIC ACID 1% WITH ACNE MEDICATION

OTC - PURPOSE SECTION


Acne medication



  • For the treatment and management of acne
  • reduces the number of acne pimples and blackheads and allows the skin to heal
  • helps to prevent new acne pimples from forming











OTC - WHEN USING SECTION


FOR EXTERNAL USE ONLY

Allergy alert:

do not use this product it you have a known allergy to salicylic acid.



  • Cleanse the skin thoroughly before applying medication
  • use the pad to wipe the entire affected area
  • repeat with a clean pad as necessary to remove remaining traces of dirt,because excessive drying of the skin may occur , start with one application
               daily , then gradually increase to two to three times daily as needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day
  • do not leave pad on skin for an extended period of time
  • keep away from eyes ,lips and other mucous membrane

using other topical acne medications at the same time or immediately following use of this product may increase
dryness or irritation of the skin. If this occurs , only one medication should be used unless directed by doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


If swallowed get get medical help or contact a posion control center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL



Naturally Clear

Stridex
Stridex label
Stridex label


The Natural acne solution with the proven effectiveness of stridex












DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
883808salicylic acid 1 % Medicated PadPSN1
968100Stridex 1 % Medicated PadPSN1
968100salicylic acid 10 MG/ML Medicated Pad [Stridex]SBD1
883808salicylic acid 10 MG/ML Medicated PadSCD1
883808salicylic acid 1 % Medicated PadSY1
968100Stridex 1 % Medicated PadSY1
968100Stridex 10 MG/ML Medicated PadSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZOIC ACID Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10157-1070-12019-10-21C16284748780-1956f9ecf-d752-621f-e053-dbdaa90a74adDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10157-1070-1STRIDEXNaturally Clear70 in 1 JARLIQUID701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10157-1070STRIDEX NATURALLY CLEAR LIQUID [BLISTEX INC ]1Legacy NDC, 1 package rows20100111_b3a78318-293a-4869-b442-3b6a9965791f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ1
BENZOIC ACIDACTIVE MOIETY8SKN0B0MIM1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10157-107010157-1070-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
eb9d76fe-ae97-4cf4-9efe-95613109df1bb3a78318-293a-4869-b442-3b6a9965791f2009-11-23Exact identifier
spl id: eb9d76fe-ae97-4cf4-9efe-95613109df1b
spl set id: b3a78318-293a-4869-b442-3b6a9965791f

Reported adverse events (FAERS/openFDA)#

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