PHARMACYS PRESCRIPTION 8 OZ ACNE CONTROL

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date
2022-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:13:04

Label at a glance#

ProductPHARMACYS PRESCRIPTION 8 OZ ACNE CONTROL
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

for the treatment of acne.

Dosage and administration

Wash face as you normally would and pat dry with a clean towel. Apply a small amount to cotton ball or pad and apply 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. If bothersome drying or peeling occurs, reduce application.

Label contents#

Full prescribing information#

Drug Facts Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.5%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Uses

INDICATIONS & USAGE SECTION

for the treatment of acne.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from open flame.

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 once medication should be used, unless directed by a doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Wash face as you normally would and pat dry with a clean towel.
  • Apply a small amount to cotton ball or pad and apply 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.
  • If bothersome drying or peeling occurs, reduce application.

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-12876176-128-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
d6138877-77ab-5336-e053-2995a90a028fd6138877-77ac-5336-e053-2995a90a028f2022-01-01WarningsExact identifier
spl id: d6138877-77ab-5336-e053-2995a90a028f
spl set id: d6138877-77ac-5336-e053-2995a90a028f

Reported adverse events (FAERS/openFDA)#

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