FDA.reportPublic FDA data

SUPPORT SERUM FORTIFIED

Manufacturer
ZENMED Raging Creations Ltd. | Sun Deep Inc.
Effective date
2025-11-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:43:05

Label at a glance#

ProductSUPPORT SERUM FORTIFIED
Active ingredientSULFUR
Label structure9 sections

Indications and uses

HELPS CLEAR UP ACNE PIMPLES, WHITEHEADS AND BLACKHEADS AND ALLOWS SKIN TO HEAL. HELPS PREVENT NEW ACNE BLEMISHES FROM FORMING. PENETRATES PORES TO CONTROL ACNE PIMPLES, BLACKHEADS AND WHITEHEADS.

Dosage and administration

- CLEANSE THE SKIN THOROUGHLY BEFORE APPLYING THIS PRODUCT - COVER THE ENTIRE AFFECTED AREA ONCE DAILY - BECAUSE EXCESSIVE DRYING OF THE SKIN MAY OCCUR, START WITH ONE APPLICATION DAILY AS DIRECTED BY A DOCTOR. CAN BE INCREASED TO UP TO 3 TIMES PER DAY - IF BOTHERSOME DRYNESS OR PEELING OCCURS, REDUCE APPLICATION EVERY OTHER DAY. FOLLOW WITH DESIRED MOISTURIZER. SENSITIVITY TEST FOR A NEW USER: APPLY PRODUCT SPARI...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

4% COLLOIDAL SULFUR

PURPOSE

OTC - PURPOSE SECTION

ACNE TREATMENT CREAM.

USES

INDICATIONS & USAGE SECTION

HELPS CLEAR UP ACNE PIMPLES, WHITEHEADS AND BLACKHEADS AND ALLOWS SKIN TO HEAL. HELPS PREVENT NEW ACNE BLEMISHES FROM FORMING. PENETRATES PORES TO CONTROL ACNE PIMPLES, BLACKHEADS AND WHITEHEADS.

WARNINGS

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

FOR EXTERNAL USE ONLY. DO NOT USE ON - BROKEN SKIN - LARGE AREAS OF THE SKIN.

OTC - WHEN USING SECTION

WHEN USING THIS PRODUCT - APPLY ONLY TO AREAS WITH ACNE. WHEN USING THIS PRODUCT - SKIN IRRITATION AND 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 - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

- CLEANSE THE SKIN THOROUGHLY BEFORE APPLYING THIS PRODUCT - COVER THE ENTIRE AFFECTED AREA ONCE DAILY - BECAUSE EXCESSIVE DRYING OF THE SKIN MAY OCCUR, START WITH ONE APPLICATION DAILY AS DIRECTED BY A DOCTOR. CAN BE INCREASED TO UP TO 3 TIMES PER DAY - IF BOTHERSOME DRYNESS OR PEELING OCCURS, REDUCE APPLICATION EVERY OTHER DAY. FOLLOW WITH DESIRED MOISTURIZER. SENSITIVITY TEST FOR A NEW USER: APPLY PRODUCT SPARINGLY TO ONE OR TWO SMALL, AFFECTED AREAS DURING THE FIRST 3 DAYS. IF NO DISCOMFORT OCCURS, FOLLOW THE DIRECTIONS STATED.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, CAPRYLIC/CAPRIC TRIGLYCERIDE, DICAPRYLYL CARBONATE, GLYCERYL STEARATE, CETYL ALCOHOL, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, SQUALANE, POLYSORBATE 60, AVOCADO SEED OIL, GLYCERIN, PENTAPEPTIDE-59. HYDROGENATED LECITHIN, SHEA BUTTER1, PHENETHYL ALCOHOL, ETHYLHEXYLGLYCERIN, MALTODEXTRIN, STEARIC ACID, GLYCERYL STEARATE CITRATE, STEARYL ALCOHOL, 1,2-HEXANEDIOL, CAPRYLYL GLYCOL, BIXA ORELLANA SEED EXTRACT, VITAMIN E, MEADOWSWEET FLOWER EXTRACT, GREEN TEA LEAF EXTRACT1, CUCUMBER EXTRACT1, & HYALURONIC ACID.

1 DENOTES CERTIFIED ORGANIC INGREDIENT

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

CALL: 1-888-749-4998
VISIT: ZENMED.COM
EMAIL: INFO@ZENMED.COM

PRINCIPAL DISPLAY PANEL - 60 ML Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SUPPORT
SERUM
FORTIFIED

Extra Strength,
Medicated
Formula

With Natural
Extracts to Clear
Troubled Skin

VEGAN,
PLANT-BASED

CRUELTY-FREE
CERTIFIED

60 ML | 2 fl OZ

ZENMED®
Reconstructive Skincare

Principal Display Panel - 60 ML Bottle Label
Principal Display Panel - 60 ML Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247817sulfur 4 % Topical CreamPSN1
247817sulfur 40 MG/ML Topical CreamSCD1
247817sulfur 4 % Topical CreamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83313-0064-1SUPPORT SERUM FORTIFIED60 mL in 1 BOTTLECREAM601

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83313-006483313-0064-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
SULFUR70FD1KFU70ACTIB
WATER059QF0KO0RIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
CETYL ALCOHOL936JST6JCNIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%)86FQE96TZ4IACT
SQUALANEGW89575KF9IACT
POLYSORBATE 60CAL22UVI4MIACT
GLYCERINPDC6A3C0OXIACT
PENTAPEPTIDE-59D8G3WTU93ZIACT
SHEA BUTTERK49155WL9YIACT
PHENYLETHYL ALCOHOLML9LGA7468IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
MALTODEXTRIN7CVR7L4A2DIACT
STEARIC ACID4ELV7Z65APIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
STEARYL ALCOHOL2KR89I4H1YIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
CAPRYLYL GLYCOL00YIU5438UIACT
BIXA ORELLANA SEEDO87354RZ5AIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CUCUMBERYY7C30VXJTIACT
HYALURONIC ACIDS270N0TRQYIACT

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
SUPPORT SERUM FORTIFIEDSULFURZENMED Raging Creations Ltd.26e5777d-4ce2-458c-90f1-4c23c7b571ed2025-11-10WarningsExact identifier
ndc (package): 83313-0064-1
ndc (product): 83313-0064
ndc11 (package): 83313006401
spl id: c32744c8-8b75-4e65-b0c0-ce50e81423bd
spl set id: 26e5777d-4ce2-458c-90f1-4c23c7b571ed

Reported adverse events (FAERS/openFDA)#

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