FDA.reportPublic FDA data

EradiKate Daily Foaming Cleanser

Manufacturer
Rare Beauty Brands Inc.
Effective date
2025-12-01
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:18:50

Label at a glance#

ProductEradiKate Daily Foaming Cleanser Acne Treatment
Active ingredientSULFUR
Label structure11 sections

Indications and uses

FOR THE TRETAMENT OF ACNE HELPS KEEP SKIN CLEAR OF NEW ACNE BLEMISHES

Dosage and administration

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 EXCESSIVE DRYNESS 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 OC...

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

SULFUR  3.0%

PURPOSE

OTC - PURPOSE SECTION

ACNE TREATMENT

USES

INDICATIONS & USAGE SECTION

  • FOR THE TRETAMENT OF ACNE
  • HELPS KEEP SKIN CLEAR OF NEW ACNE BLEMISHES

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY

OTC - WHEN USING SECTION

WHEN USING THIS PRODUCT

  • 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

STOP USE AND ASK A DOCTOR IF RASH OCCURS.

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

  • 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 EXCESSIVE DRYNESS 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.

OTHER INFORMATION

OTHER SAFETY INFORMATION

  • STORE IN A COOL, DRY PLACE. AVOID PRODUCT CONTACT WITH SILVER JEWELRY, WHICH MAY BE DISCOLORED BY THIS PRODUCT.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER/AQUA/EAU, SODIUM COCOYL ISETHIONATE, COCO-GLUCOSIDE, ACRYLATES COPOLYMER, COCONUT ALCOHOL, GLYCERETH-18 ETHYLHEXANOATE, GLYCERETH-18, STEARYL ALCOHOL, HONEY EXTRACT/MEL/EXTRAIT DE MIEL, ORYZA SATIVA (OAT) KERNEL EXTRACT, OLIGOPEPTIDE-10, BOSWELLIA SERRATA EXTRACT, BEHENYL ALCOHOL, GLYCERIN, PHENOXYETHANOL, FRAGRANCE/PARFUM, CITRIC ACID, SODIUM HYDROXIDE, ETHYLHEXYLGLYCERIN, DISODIUM EDTA, DISODIUM CARBOXYETHYL SILICONATE, TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77491)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0-UC_EradiKate Cleanser_120mL0-UC_EradiKate Cleanser_120mL

0-LBL_EradiKate Cleanser_120mL0-LBL_EradiKate Cleanser_120mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046894sulfur 3 % Medicated Liquid SoapPSN9
1046894sulfur 30 MG/ML Medicated Liquid SoapSCD9
1046894sulfur 3 % Medicated Liquid SoapSY9

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72204-902-01EradiKate Daily Foaming CleanserAcne Treatment120 mL in 1 TUBEGEL1209
72204-902-02EradiKate Daily Foaming CleanserAcne Treatment1 in 1 BOXGEL19
72204-902-03EradiKate Daily Foaming CleanserAcne Treatment50 mL in 1 TUBEGEL509
72204-902-04EradiKate Daily Foaming CleanserAcne Treatment30 mL in 1 TUBEGEL309
72204-902-05EradiKate Daily Foaming CleanserAcne Treatment240 mL in 1 TUBEGEL2409

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72204-90272204-902-01, 72204-902-02, 72204-902-03, 72204-902-04, 72204-902-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM COCOYL ISETHIONATE518XTE8493IACT
COCO GLUCOSIDEICS790225BIACT
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
COCONUT ALCOHOL13F4MW8Y9KIACT
GLYCERETH-18 ETHYLHEXANOATEIWS58C6V2YIACT
GLYCERETH-18SA5E43C17CIACT
STEARYL ALCOHOL2KR89I4H1YIACT
HONEYY9H1V576FHIACT
ORYZA SATIVA WHOLE84IVV0906ZIACT
AVENA SATIVA WHOLE5P8D0Z74RGIACT
OLIGOPEPTIDE-10Q46328TRNKIACT
BOSWELLIA SERRATA WHOLEX7B7P649WQIACT
DOCOSANOL9G1OE216XYIACT
GLYCERINPDC6A3C0OXIACT
XANTHAN GUMTTV12P4NEEIACT
CAPRYLYL GLYCOL00YIU5438UIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
SODIUM HYDROXIDE55X04QC32IIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
EDETATE DISODIUM7FLD91C86KIACT
DISODIUM CARBOXYETHYL SILICONATE4U4C79679GIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FERRIC OXIDE RED1K09F3G675IACT
SULFUR70FD1KFU70ACTIB

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
EradiKate Daily Foaming Cleanser Acne TreatmentSULFURRare Beauty Brands Inc.44ebc725-796f-71e6-e063-6294a90a69a62025-12-01WarningsExact identifier
ndc (package): 72204-902-01
ndc (package): 72204-902-02
ndc (package): 72204-902-03
ndc (package): 72204-902-04
ndc (package): 72204-902-05
ndc (product): 72204-902
ndc11 (package): 72204090202
ndc11 (package): 72204090201
ndc11 (package): 72204090205
ndc11 (package): 72204090204
ndc11 (package): 72204090203
spl id: 44ebc725-796e-71e6-e063-6294a90a69a6
spl set id: 44ebc725-796f-71e6-e063-6294a90a69a6

Reported adverse events (FAERS/openFDA)#

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