Dr.zium All Clear Spot

Manufacturer
GM Holdings Co., Ltd | Cosmax, Inc.
Effective date
2018-01-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:54:13

Label at a glance#

ProductDr.zium All Clear Spot
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid

INACTIVE INGREDIENT SECTION

Niacinamide, Terminalia Ferdinandiana Fruit Extract, Aazelaoyl Octapeptide-9, Water, etc

OTC - PURPOSE SECTION

Acne Treatment

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Apply an adequate amount to the trouble area and absorb with gentle dabbing

WARNINGS SECTION

Warnings

Do not use if you have very sensitive skin or are sensitive to Salicylic Acid

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

For external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69278-001-012022-01-28C16284748780-1d6a99b39-b712-a426-e053-dadaa90af4c263061155-c48e-5bd8-e053-2a91aa0a2e8d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69278-001-01Dr.zium All Clear Spot15 mL in 1 TUBECREAM152

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69278-001DR.ZIUM ALL CLEAR SPOT (SALICYLIC ACID) CREAM [GM HOLDINGS CO., LTD]2Legacy NDC, 1 package rows20180122_63061155-c48e-5bd8-e053-2a91aa0a2e8d.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69278-00169278-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
6357a81a-6e7b-3c07-e053-2991aa0a94e463061155-c48e-5bd8-e053-2a91aa0a2e8d2018-01-22WarningsExact identifier
spl id: 6357a81a-6e7b-3c07-e053-2991aa0a94e4
spl set id: 63061155-c48e-5bd8-e053-2a91aa0a2e8d

Reported adverse events (FAERS/openFDA)#

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