FDA.reportPublic FDA data

Stridex XL Face and Body Pads

Manufacturer
Blistex Inc
Effective date
2024-12-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:43:39

Label at a glance#

ProductStridex XL Face and Body Pads
Active ingredientSalicylic Acid
Label structure9 sections

Indications and uses

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

Dosage and administration

clean the skin thoroughly before applying this product use the pad to cover the entire affected area with a thin layer one to three times daily because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if 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 le...

Storage and handling

DO NOT FLUSH - discard pad in trash and wash hands after use

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 2.0% (w/w)

Purpose

OTC - PURPOSE SECTION

Acne medication

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Allergy alert

SPL UNCLASSIFIED SECTION

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

When using this product

OTC - WHEN USING SECTION

  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the skin thoroughly before applying this product
  • use the pad to cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if 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 membranes

Other information

STORAGE AND HANDLING SECTION

  • DO NOT FLUSH - discard pad in trash and wash hands after use

Inactive ingredients

INACTIVE INGREDIENT SECTION

ammonium lauryl sulfate, ammonium xylenesulfonate, citric acid, citrus grandis (grapefruit) fruit extract, ethylhexylglycerin, fragrances, glycerin, menthol, phenoxyethanol, purified water, simethicone, sodium borate, tetrasodium EDTA

PRINCIPAL DISPLAY PANEL - 90 Pad Jar Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

✓ Cleans
✓ Treats
✓ Prevents

67% Bigger Pad*

ALCOHOL
FREE

STRIDEX®
SALICYLIC ACID 2% W/W ACNE MEDICATION

XL FACE & BODY PADS™

Max Strength
Medication
+
Pore Tightening
Grapefruit Extract

90 Dual Textured Pads
One Side Scrubbing • One Side Gentle

PRINCIPAL DISPLAY PANEL - 90 Pad Jar Carton
PRINCIPAL DISPLAY PANEL - 90 Pad Jar Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797892salicylic acid 2 % Medicated PadPSN3
1425554Stridex 2 % Medicated PadPSN3
1425554salicylic acid 20 MG/ML Medicated Pad [Stridex]SBD3
797892salicylic acid 20 MG/ML Medicated PadSCD3
797892salicylic acid 2 % Medicated PadSY3
797892salicylic acid 2 % Topical SwabSY3
1425554Stridex 2 % Medicated PadSY3
1425554Stridex 20 MG/ML Medicated PadSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10157-2114-1Stridex XL Face and Body Pads90 in 1 JARLIQUID903
10157-2114-1Stridex XL Face and Body Pads1 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10157-2114STRIDEX XL FACE AND BODY PADS (SALICYLIC ACID) LIQUID [BLISTEX INC]3Current NDC, Legacy NDC, 2 package rows20241215_ed459e80-22cc-40ef-862c-1adf82da2377.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10157-211410157-2114-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
Salicylic AcidO414PZ4LPZACTIB
water059QF0KO0RIACT
sodium borate91MBZ8H3QOIACT
.ALPHA.-CHLOROHYDRINQGS78A3T6PIACT
pummeloET1TN5W71XIACT
ammonium lauryl sulfateQ7AO2R1M0BIACT
ammonium xylenesulfonate4FZY6L6XCMIACT
citric acid monohydrate2968PHW8QPIACT
phenoxyethanolHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
silicon dioxideETJ7Z6XBU4IACT
edetate sodiumMP1J8420LUIACT

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
Stridex XL Face and Body PadsSALICYLIC ACIDBlistex Inced459e80-22cc-40ef-862c-1adf82da23772024-12-13WarningsExact identifier
ndc (package): 10157-2114-1
ndc (product): 10157-2114
ndc11 (package): 10157211401
spl id: 2d206763-baa2-4d21-aa28-008b84dcaf05
spl set id: ed459e80-22cc-40ef-862c-1adf82da2377

Reported adverse events (FAERS/openFDA)#

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