CLIXIT ACNE SPOT TREATMENT

Manufacturer
Renu Laboratories, Inc. | Renu Laboratories, Inc
Effective date
2019-10-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:08:41

Label at a glance#

ProductCLIXIT ACNE SPOT TREATMENT
Active ingredientSULFUR
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Sulfur 10 percent

OTC - PURPOSE SECTION

Purpose

Acne Treatment

INDICATIONS & USAGE SECTION

Use For

For the treatment of acne

WARNINGS SECTION

Warnings

For external use only

Using other topical acne medications at the same time may increase dryness or irritation of the skin. Because 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 per day.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, contact physician or poison control center immediately.

OTHER SAFETY INFORMATION

Store at room temperature

DOSAGE & ADMINISTRATION SECTION

Directions

Clean the skin thoroughly before using. Apply directly to blemish or affected area. Do not use on broken skin or large areas of the skin. For best results, use 2-3 times per day.

OTC - DO NOT USE SECTION

Do not use on broken skin or large areas of skin.

INACTIVE INGREDIENT SECTION

Other Ingredients

Camphor, Carbomer, Deionized Water, EDTA (Ethylenediamine Tetraacetic Acid), Ethanol, Ethylhexylglycerin, Phenoxyethanol, Propylene Carbonate, Salicylic Acid, Triethanolamine (TEA)

INACTIVE INGREDIENT SECTION

Other Ingredients

Camphor, Carbomer, Deionized Water, EDTA (Ethylenediamine Tetraacetic Acid), Ethanol, Ethylhexylglycerin, Phenoxyethanol, Propylene Carbonate, Salicylic Acid, Triethanolamine (TEA)

OTC - QUESTIONS SECTION

QUESTIONS

Call 844 425 4948

STATEMENT OF IDENTITY SECTION

ACNE SPOT TREATMENT

WITH 10 percent sulfur

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Acne Spot Treatment BoxAcne Spot Treatment Box

OUTER BOX FINALOUTER BOX FINAL

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-44676348-446-01, 76348-446-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
b8b8b73d-e302-f7ce-e053-2995a90a5f4d93f3ad1b-7cdb-4399-e053-2995a90aa4272021-01-12WarningsExact identifier
spl set id: 93f3ad1b-7cdb-4399-e053-2995a90aa427

Reported adverse events (FAERS/openFDA)#

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