D Acne Cream

Manufacturer
Adven Biotech Private Limited
Effective date
2016-03-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:07:39

Label at a glance#

Productd-acne
Active ingredientTHUJA OCCIDENTALIS ROOT, MAHONIA AQUIFOLIUM ROOT, CALENDULA OFFICINALIS FLOWER
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Adults: Apply externally twice daily to properly cleaned & dried affected portion.

Children under 18 years: As prescribed by the physician.

WARNINGS SECTION

If symptons persist or worsen, a physician should be consulted. Keep out of reach of children. Do not use, if known sentivity to any of its ingredients exists. In case of emergency, contact a medical professional or posion control center immediately. For external use only. Replace cap tightly.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

Controls Acne

Skin Treatment

INACTIVE INGREDIENT SECTION

Alcohol content, Cream base

OTC - ACTIVE INGREDIENT SECTION

Berberis Aquifolium, Thuja Occidentalis, Calendula Officinalis

INDICATIONS & USAGE SECTION

Treats acne, pimples, blotches, brown spots and dark discoloration of skin. Prevents suppuration.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DAcneCreamDAcneCream

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69825-005-022020-01-31C16284748780-19d75b9d0-776e-f424-e053-dadaa90a57ceD Acne Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69825-005-01d-acne30 g in 1 TUBEOINTMENT301
69825-005-02d-acne1 in 1 BOXOINTMENT11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69825-005D-ACNE (BERBERIS AQUIFOLIUM, THUJA OCCIDENTALIS, CALENDULA OFFICINALIS) OINTMENT [ADVEN BIOTECH PRIVATE LIMITED]1Legacy NDC, 2 package rows20160330_2efb2514-e161-09f2-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69825-00569825-005-01, 69825-005-02

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
2efb2514-e162-09f2-e054-00144ff8d46c2efb2514-e161-09f2-e054-00144ff8d46c2016-03-28WarningsExact identifier
spl id: 2efb2514-e162-09f2-e054-00144ff8d46c
spl set id: 2efb2514-e161-09f2-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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