CLIXIT Tinted Blemish Concealer Light Shade

Manufacturer
Renu Laboratories, Inc.
Effective date
2019-09-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:10:04

Label at a glance#

ProductCLIXIT Tinted Blemish Concealer Light Shade
Active ingredientSULFUR
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Sulfur 4%

OTC - PURPOSE SECTION

Purpose

Acne Treatment

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, contact physician or poison control center immediately.

OTC - QUESTIONS SECTION

QUESTIONS?

Call 844 425 4948

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 doctor. If bothersome dryness or peeling occurs, reduce application to once per day.

Use For:

INDICATIONS & USAGE SECTION

For the treatment of acne.

DOSAGE & ADMINISTRATION SECTION

Directions:

Clean the skin thoroughly before using. Cover entire affected area. Do not use on broken skin or large areas of the skin. For best results use 2-3 times per day.

Other Ingredients:

INACTIVE INGREDIENT SECTION

Bentonite, Cannabis Sativa (Hemp) Seed Oil, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Deionized Water, Euphorbia Cerifera (Candelilla) Wax, Glycerol Monostearate, Hippophae Rhamnoides (SeaBerry) Fruit and Seed Oil, Iron Oxide, Phenoxyethanol, Steareth-20, Titanium Dioxide, Zinc Oxide.

STATEMENT OF IDENTITY SECTION

TINTED BLEMISH CONCEALER

LIGHT SHADE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TINTED BLEMISH CONCEALER TUBE

CLIP BLEMISH CONCEALERCLIP BLEMISH CONCEALER

CLIXIT TintedBlemishConcealer LIGHT

CLIXIT LIGHT BOXCLIXIT LIGHT BOX

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-44276348-442-01, 76348-442-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
b8b89bc6-9b2f-5b65-e053-2995a90afe7a92d78404-9a78-11ca-e053-2995a90a0aab2021-01-12WarningsExact identifier
spl set id: 92d78404-9a78-11ca-e053-2995a90a0aab

Reported adverse events (FAERS/openFDA)#

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