Kate Summerville EradiKate

Manufacturer
Beauty Manufacturing Solutions Corp.
Effective date
2022-02-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:08:47

Label at a glance#

ProductKate Summerville EradiKate
Active ingredientSULFUR
Label structure12 sections

Storage and handling

Store in a cool, dry place. Avoid product contactwith silver jewelry, which may be discolored by this product.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sulfur 3.0%

Purpose: Anti-Acne active ingredient

OTC - PURPOSE SECTION

Acne Treatment

INDICATIONS & USAGE SECTION

  • For the treatment of acne
  • Helps keep skin clear of new acne blemishes

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

Skin irritation or dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

OTC - STOP USE SECTION

if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Posion Control Center right away.

DOSAGE & ADMINISTRATION SECTION

  • AM and PM. Use twice a day. Apply a small amount to wet face and massage gently for 30 seconds. Rinse and gently pat dry. Avoid contact with eye area. Follow with EradiKate Acne Treatment for maximum results.
  • Because of excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
  • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

INACTIVE INGREDIENT SECTION

Aqua/Water/Eau, Sodium Cocoyl Isethionate, Coco-Glucoside, Acrylates Copolymer, Coconut Alcohol, Glycereth-18 Ethylhexanoate, Glycereth-18, Stearyl Alcohol, Honey Extract, Oryza Sativa (Rice) Bran Extract, Avena Sativa (Oat) Kernel Extract, Oligopeptide-10, Boswellia Serrata Extract, Behenyl Alcohol, Glycerin, Xanthan Gum, Caprylyl Glycol, Hexylene Glycol, Butylene Glycol, Phenoxyethanol, Fragrance (Parfum), Citric Acid, Sodium Hydroxide, Ethylhexylglycerin, Disodium EDTA, Disodium Carboxyethyl Siliconate, Titanium Dioxide (CI 77891), Iron Oxides (CI 77491)

STORAGE AND HANDLING SECTION

Store in a cool, dry place. Avoid product contactwith silver jewelry, which may be discolored by this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principle Display PanelPrinciple Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11090-26311090-263-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d7c14c78-737f-5f38-e053-2a95a90a1ba0d4b15ecd-ecdf-a8e0-e053-2995a90ad40a2022-02-11WarningsExact identifier
spl id: d7c14c78-737f-5f38-e053-2a95a90a1ba0
spl set id: d4b15ecd-ecdf-a8e0-e053-2995a90ad40a

Reported adverse events (FAERS/openFDA)#

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