Pharmacys Prescription 8 OZ Acne Control

Manufacturer
American Consumer Products Corp
Effective date
2019-09-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:00:27

Label at a glance#

ProductPharmacys Prescription 8 OZ Acne Control
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

Directions: Wash face as you normally would and pat dry with a clean towel. Apply a small amount to cotton ball or pad and applyu using a dabbing motion. Take care to avoid rubbing in eyes. Use astringent two to three times daily or as directed by your doctor to keep your skin clear and healthy. Apply a light moisturizer after using astringent.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient: Salicylic Acid 0.5%

Purpose

OTC - PURPOSE SECTION

Purpose: Acne treatment

Uses: for the treatment of acne.

Warnings

WARNINGS SECTION

Warnings: For external use only.

Flammable, keep away from open flame.

Keep out of reach of children

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 immediately.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), Alcohol (24.5%), Propylene Glycol, Glycerin, PEG-32, Algae Extract, DMDM Hydantoin, Dimethicone Propyl PG-Betaine, Sodium Citrate, Aloe Barbadensis Leaf Extract, Benzophenone-4, Denatonium Benzoate, Fragrance, FD&C Yellow No..5.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: Wash face as you normally would and pat dry with a clean towel. Apply a small amount to cotton ball or pad and applyu using a dabbing motion. Take care to avoid rubbing in eyes. Use astringent two to three times daily or as directed by your doctor to keep your skin clear and healthy. Apply a light moisturizer after using astringent.

INSTRUCTIONS FOR USE SECTION

When using this product

- avoid contact with eyes. If contact occurs, immediately flush with water.

- 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 a doctor.

Indications & Usage

INDICATIONS & USAGE SECTION

If bothersome drying or peeling occurs, reduce application.

Pharmacys Prescription 8 OZ Acne Control

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pharmacys Prescription Acne ControlPharmacys Prescription Acne Control

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-015-082023-01-30C16284748780-1f386c649-a5fe-0266-e053-dadaa90a7c1aPharmacys Prescription 8 OZ Acne Control

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-015-08Pharmacys Prescription 8 OZ Acne Control236.58 mL in 1 BOTTLELIQUID236.581

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-015PHARMACYS PRESCRIPTION 8 OZ ACNE CONTROL (SALICYLIC ACID) LIQUID [AMERICAN CONSUMER PRODUCTS CORP]1Legacy NDC, 1 package rows20190917_914a2512-8a3a-7771-e053-2a95a90a72e3.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72197-01572197-015-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
914a2512-8a3b-7771-e053-2a95a90a72e3914a2512-8a3a-7771-e053-2a95a90a72e32019-09-16WarningsExact identifier
spl id: 914a2512-8a3b-7771-e053-2a95a90a72e3
spl set id: 914a2512-8a3a-7771-e053-2a95a90a72e3

Reported adverse events (FAERS/openFDA)#

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