FDA.reportPublic FDA data

CLIXIT TINTED BLEMISH CONCEALER MEDIUM SHADE

Manufacturer
RENU LABORATORIES, INC. | RENU LABORATORIES
Effective date
2019-09-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:09:57

Label at a glance#

ProductCLIXIT TINTED BLEMISH CONCEALER MEDIUM SHADE
Active ingredientSULFUR
Label structure10 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sulfur 4%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, contact physician or poison control center immediately.

QUESTIONS ?

OTC - QUESTIONS SECTION

Call 844 425 4948

Warnings

WARNINGS SECTION

For external use only.

Using other topical care 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.

INDICATIONS & USAGE SECTION

For the treatment of acne.

Directions:

DOSAGE & ADMINISTRATION SECTION

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

MEDIUM SHADE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLIP BLEMISH CONCEALER

CLIP BLEMISH CONCEALERCLIP BLEMISH CONCEALER

CLIXIT_MEDIUM_TintedBlemishConcealer_MEDIUM_BOX_

CLIXIT MEDIUM BOXCLIXIT MEDIUM BOX

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-44376348-443-01, 76348-443-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
CANDELILLA WAXWL0328HX19IACT
CETYL ALCOHOL936JST6JCNIACT
BROWN IRON OXIDE1N032N7MFOIACT
SULFUR70FD1KFU70ACTIB
WATER059QF0KO0RIACT
BENTONITEA3N5ZCN45CIACT
ZINC OXIDESOI2LOH54ZIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
HIPPOPHAE RHAMNOIDES SEED OILT53SBG6741IACT
CORN OIL8470G57WFMIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
STEARETH-10FD0913P475IACT
STEARETH-20L0Q8IK9E08IACT
HIPPOPHAE RHAMNOIDES FRUIT OILTA4JCF9S1JIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PHENOXYETHANOLHIE492ZZ3TIACT

Source Document#

Source XML · Source PDF

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
b8b8ff85-6f4a-e6c3-e053-2a95a90ae5ce933f825c-6274-e9d5-e053-2a95a90ada0e2021-01-12WarningsExact identifier
spl set id: 933f825c-6274-e9d5-e053-2a95a90ada0e

Reported adverse events (FAERS/openFDA)#

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