Label: CLIXIT TINTED BLEMISH CONCEALER MEDIUM- sulfur cream
-
Contains inactivated NDC Code(s)
NDC Code(s): 71328-045-01, 71328-045-02 - Packager: Clixit, Llc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 17, 2021
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Use:
-
Warnings:
For external use only.
When using this product
• Do not use on broken skin or large areas of skin
• Apply only to areas with acne
• 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 - Directions:
- Other Ingredients:
-
SPL UNCLASSIFIED SECTION
with 4% sulfur, hemp & cloudberry
Conceal & Heal
Tinted mineral formula conceals acne while it allows skin to heal
MEDIUM/DARK
SKINCARE BY CLIXIT®
CONCEALS WHILE IT HEALS ACNE BLEMISHES
Powerful, natural ingredients such as Hemp, Cloudberry, Zinc Oxide, and Sulfur help heal acne blemishes while it conceals
Covers, soothes and calms problem skin, redness, rashes and other forms of dermatitis
TINTED MINERAL ACNE CONCEALING AND SKIN-HEALING FORMULA is ideal for all skin types
QUESTIONS?
Call 844-425-4948Made in the USA
Distributed by
Clixit, LLC, Orlando, FLNOT TESTED ON ANIMALS
- Packaging
-
INGREDIENTS AND APPEARANCE
CLIXIT TINTED BLEMISH CONCEALER MEDIUM
sulfur creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71328-045 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BENTONITE (UNII: A3N5ZCN45C) CANDELILLA WAX (UNII: WL0328HX19) CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) PHENOXYETHANOL (UNII: HIE492ZZ3T) RUBUS CHAMAEMORUS SEED OIL (UNII: WH495F04LZ) STEARETH-20 (UNII: L0Q8IK9E08) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) ZINC OXIDE (UNII: SOI2LOH54Z) Product Characteristics Color brown (Light Brown) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71328-045-02 1 in 1 BOX 02/01/2021 1 NDC:71328-045-01 15 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 02/01/2021 Labeler - Clixit, Llc (014971694)