CLIXIT ACNE DRYING LOTION

Manufacturer
Renu Laboratories, Inc. | Renu Laboratories
Effective date
2019-10-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:08:36

Label at a glance#

ProductClixit Skin Care Acne Drying
Active ingredientSULFUR
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Sulfur Colloidal 10%

OTC - PURPOSE SECTION

Purpose

Acne Treatment

INDICATIONS & USAGE SECTION

Use

For treatment of acne. Healing and drying of acne. Penetrates pores to control acne. Helps prevent breakouts.

WARNINGS SECTION

Warnings

For external use only

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.

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. Cover affected areas with thin layer two or three times a day

OTC - DO NOT USE SECTION

Do not use on broken skin or large areas of skin. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Camphor, Deionized Water, Hippophae Rhamnoides (Seaberry) Fruit and Seed Oil, Iron Oxide, Isopropyl Alcohol, Magnesium Aluminum Silicate, Salicylic Acid, Zinc Oxide.

OTC - QUESTIONS SECTION

QUESTIONS

Call 844 425 4948

STATEMENT OF IDENTITY SECTION

Outer Box

DRYING LOTION BOXDRYING LOTION BOX

RECENT MAJOR CHANGES SECTION

The only change was the removal of a punctuation mark in the Dosage and Administration section

10/2019

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drying Lotion Label

Clixit Drying Lotion LabelClixit Drying Lotion Label

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-44776348-447-01, 76348-447-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
ba765504-9249-ec13-e053-2a95a90a0b569405f298-f038-1ca8-e053-2a95a90a307d2021-02-03WarningsExact identifier
spl set id: 9405f298-f038-1ca8-e053-2a95a90a307d

Reported adverse events (FAERS/openFDA)#

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