CLIXIT ® ACNE DRYING LOTION

Manufacturer
Clixit, Llc
Effective date
2021-04-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:53

Label at a glance#

ProductCLIXIT ACNE DRYING
Active ingredientSULFUR
Label structure8 sections

Dosage and administration

DO NOT SHAKE BOTTLE . Clean the skin thoroughly before using at night. Apply only to areas with acne. Allow solution to dry and rinse off in the morning. Do not use on broken skin or large areas of skin. If bothersome dryness or peeling occurs, reduce application to every other day.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sulfur 10%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Use:

INDICATIONS & USAGE SECTION

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

Warnings:

WARNINGS SECTION

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.Stop use and ask a doctor if skin irritation occurs or gets worse. Rinse right away with water if product gets in eyes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, get medical help or call a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

DO NOT SHAKE BOTTLE.
Clean the skin thoroughly before using at night. Apply only to areas with acne. Allow solution to dry and rinse off in the morning.

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Allantoin, Aqua (Deionized Water), Camphor, Ethylhexylglycerin, Iron Oxide, Isopropyl Alcohol, Magnesium Aluminium Silicate, Phenoxyethanol, Salicylic Acid, Zinc Oxide.

SPL UNCLASSIFIED SECTION

Overnight Treatment

For stubborn acne

SKINCARE BY CLIXIT ®

POWERFUL SULFUR AND SALICYLIC ACID FORMULA penetrates pores and dries out stubborn acne overnight revealing smaller, less noticeable blemishes.

Clears acne and allows skin to heal

Emergency spot treatment

Reduces size of stubborn acne

Results overnight

Ideal for all skin types

POWERFUL OVERNIGHT ACNE TREATMENT

QUESTIONS?
Call 844-425-4948

Made in the USA

Distributed by
Clixit, LLC, Orlando, FL

NOT TESTED ON ANIMALS

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240725sulfur 10 % Topical LotionPSN1
240725sulfur 100 MG/ML Topical LotionSCD1
240725sulfur 10 % Topical LotionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71328-042-022024-01-30C16284748780-11030e365-603a-111a-e063-dadaa90a10e2CLIXIT ® ACNE DRYING LOTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71328-042-01CLIXIT ACNE DRYING29 mL in 1 BOTTLELOTION291
71328-042-02CLIXIT ACNE DRYING1 in 1 BOXLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71328-042CLIXIT ACNE DRYING (SULFUR) LOTION [CLIXIT, LLC]1Legacy NDC, 2 package rows20210424_16abb1bd-ed96-49b4-bf99-86b7926c4a05.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71328-04271328-042-01, 71328-042-02

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
27a724f9-5914-471d-98b9-7dca8027504f16abb1bd-ed96-49b4-bf99-86b7926c4a052021-04-16WarningsExact identifier
spl id: 27a724f9-5914-471d-98b9-7dca8027504f
spl set id: 16abb1bd-ed96-49b4-bf99-86b7926c4a05

Reported adverse events (FAERS/openFDA)#

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