dermveda ​™ ULTRA FOLLICULITIS TREATMENT CREAM

Manufacturer
Celcius Corp.
Effective date
2026-05-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-03 18:03:24

Label at a glance#

Productdermveda ULTRA FOLLICULITIS TREATMENT
Active ingredientSULFUR, TURMERIC
Label structure10 sections

Indications and uses

• Temporarily relieves swelling, itching, rash or skin irritation/inflammation.

Dosage and administration

Do Not use on Children less than 2 Years Please perform a patch test for sensitive skin. Take a small amount with your finger and gently apply it on the affected area. Apply Liberally and use often till symptoms subside.

Storage and handling

Store in a cool dry place.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sulfur 10x HPUS
Curcuma Longa 10C HPUS

Purpose

OTC - PURPOSE SECTION

Anti-Fungal
Anti-microbial

Uses

INDICATIONS & USAGE SECTION

• Temporarily relieves swelling, itching, rash or skin irritation/inflammation.

Warnings

WARNINGS SECTION

For external use only.

Do not use • on children under 2 years of age unless directed by a doctor • Avoid contact with eyes.

When using this product
• Mild increase in irritation or burning may occur.

Stop use and ask a doctor if
• Symptoms persist or inflammation increases after weeks of use or if the itch increases.
• Increase in redness on skin.

Pregnant or Breast Feeding
• Ask a Health Professional before use.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Do Not use on Children less than 2 Years
Please perform a patch test for sensitive skin. Take a small amount with your finger and gently apply it on the affected area. Apply Liberally and use often till symptoms subside.

Other information

STORAGE AND HANDLING SECTION

Store in a cool dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Azadirachta Indica, Glycerin, Hydroxyethylcellulose, Peppermint oil, Olive Oil, Karanja oil, Sweet flag oil, Sweet Indrajao oil, Xanthan Gum, Water (Aqua)

Questions?

OTC - QUESTIONS SECTION

+1-734-726-0148
You may also report serious side effects to this phone number.
Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

Extra Strength

TINEA MEDICINE

SOOTHES & RELIEVES, ITCHY, SCALY, INFLAMED SKIN

FDA REGISTERED HOMEOPATHIC MEDICINE

No Synthetics

No Parabens

No Alcohol

No Chlorides

Plant Anti-Fungal soothing cream

Distributed by:
Celcius Corp
21415 Civic center drive
Southfield, MI 48076
Sales@celcius.us

made with Love

NO ANIMAL TESTING

www.Celsiusherbs.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UltraFolliculitisTreatmentUltraFolliculitisTreatment

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

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
83819-60683819-606-02

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
dermveda ULTRA FOLLICULITIS TREATMENTSULFUR, CURCUMA LONGACelcius Corp.f43bc300-50bf-421a-81f8-1da7fc829cd02026-05-29WarningsExact identifier
ndc (package): 83819-606-02
ndc (product): 83819-606
ndc11 (package): 83819060602
spl id: 00956a31-f8e0-4aab-816f-718a19f8a8e8
spl set id: f43bc300-50bf-421a-81f8-1da7fc829cd0

Reported adverse events (FAERS/openFDA)#

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