FDA.reportPublic FDA data

Dr Berrys

Manufacturer
Nature's Innovation, Inc.
Effective date
2020-12-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:01:46

Label at a glance#

ProductDr Berrys Multi-purpose sulfur Creme
Active ingredientSULFUR
Label structure8 sections

Indications and uses

Symptomatic treatment of acne, seborrheic dermatitis, mite, and tinea fungal infections.

Dosage and administration

Cleanse skin thoroughly before applying. Cover the affected skin area with creme once per day. If excessive drying of the skin or rash occurs, reduce the application of creme or discontinue use. To speed relief, we recommend using Dr.Berry’s Sulfur Soap with Lavender. Some individuals may be sensitive to sulfur or essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Sulfur 1X HPUS

The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

Purpose:

OTC - PURPOSE SECTION

acne, seborrheic dermatitis, mite, and tinea Symptom Relief

Uses:

INDICATIONS & USAGE SECTION

Symptomatic treatment of acne, seborrheic dermatitis, mite, and tinea fungal infections.

Warnings:

WARNINGS SECTION

For external use only. Ask a doctor before use if pregnant or nursing. Avoid using near eyes, mouth or mucous membranes. If eye contact occurs, rinse thoroughly with water and consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
Do not use if tamper evident seal is broken. In case of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.

Directions:

DOSAGE & ADMINISTRATION SECTION

Cleanse skin thoroughly before applying. Cover the affected skin area with creme once per day. If excessive drying of the skin or rash occurs,
reduce the application of creme or discontinue use. To speed relief, we recommend using Dr.Berry’s Sulfur Soap with Lavender. Some
individuals may be sensitive to sulfur or essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aqua, Carbomer, Cetearyl Alcohol, Glyceryl Stearate, Helianthus Annus ( Sunflower) Seed Oil, Phenoxyethanol, Polysorbate 20,Potassium Sorbate, Sodium Hydroxide, Tea Tree Oil.

SPL UNCLASSIFIED SECTION

Est. 1892

Dr. Berry’s Multi-Purpose Sulfur Creme can be used to relieve symptoms of a variety of skin disorders including: 
acne, seborrheic dermatitis, mite infestations, or tinea fungal infections. It inhibits the growth of bacteria, has anti-fungal properties and exfoliates the skin. Dryness may occur. 

Close jar tight after each use.

Questions? Comments? 1-866-371-2499
Mfd. by: Nature’s Innovation, Inc.
5317 Palmero Ct., Buford, GA 30518

*These statements or claims are based upon traditional homeopathic practice. They have not been reviewed by the Food & Drug Administration. “X “is a homeopathic dilution.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10893-440DR BERRYS MULTI-PURPOSE SULFUR CREME (SULFUR) CREAM [NATURE'S INNOVATION, INC.]1Legacy NDC20201217_d9171e5c-edf7-4450-860f-8178a053feb8.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10893-44010893-440-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
SULFUR70FD1KFU70ACTIB
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
SUNFLOWER OIL3W1JG795YIIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM HYDROXIDE55X04QC32IIACT
TEA TREE OILVIF565UC2GIACT

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
426732c5-62e1-468a-8b1b-0c638d3aadb5d9171e5c-edf7-4450-860f-8178a053feb82025-07-25WarningsExact identifier
spl set id: d9171e5c-edf7-4450-860f-8178a053feb8

Reported adverse events (FAERS/openFDA)#

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