Colorlogix Clear and Sheer

Colorlogix Clear and Sheer by

Drug Labeling and Warnings

Colorlogix Clear and Sheer by is a Otc medication manufactured, distributed, or labeled by Induction Therapies LLC, Induction Therapies, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

COLORLOGIX CLEAR AND SHEER- it clear powder 
Induction Therapies LLC

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.

----------

Colorlogix Clear and Sheer

Side Panel Box


MINERAL POWDER SUNSCREEN mattifies shine while delivering daily sun protection. Brush it on throughout the day to reduce shine and ease SPF reapplication.


HOW TO USE
1. Remove the cap, slide down clear plastic sleeve and remove the rubber band from around the bristles
2. Pull the clear plastic sleeve back up and replace cap, then turn over and tap the cap 3-7 times to prime applicator brush
3. Activate powder flow by removing cap and fanning the bristles against your wrist
4. Generously apply powder in small circles to achieve full coverage
5. To close: pull the clear plastic sleeve up and replace the cap

Re-Activation: If your powder stops flowing, repeat step two

Drug Facts Box

DRUG FACTS:

Active Ingredients

Active Ingredients

Zinc Oxide 25%

Purpose

Sunscreen

Uses

Uses:

Helps prevent sunburn.

Warnings

Warnings:

For external use only.

Do not use on damaged or broken skin.

Stop use and ask a doctor if rash occurs.

When using this product, keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Directions:

Apply liberally to face at least 15 minutes before sun exposure.
Use a water resistant sunscreen if swimming or sweating.
Reapply at least every 2 hours.
Children under 6 months of age: Ask a doctor.

Sun Protection Measures

Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum value of 15 or higher and other sun protection measures including:

Limit time in the sun, especially from 10 a.m.-2 p.m.

Wear long-sleeved shirts, pants, hats, and sunglasses.

Inactive Ingredients

Inactive Ingredients: Sericite, Mica, and Silica.

Other Information

Protect this product from excessive heat and direct sun.

Questions or Comments?

Questions or Comments? 877.746.4407, Mon-Fri 8 a.m.-6 p.m. EST

Tube Labeling

Uses: Helps prevent sunburn.

Warnings: For external use only. Do not use on damaged or broken skin. Stop use and ask a doctor if rash occurs. When using this product, keep out of eyes. Rinse with water to remove. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions: Apply liberally to face at least 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. Children under 6 months of age: Ask a doctor.

Active Ingredients: Zinc Oxide 25%

Inactive Ingredients: Sericite, Mica, and Silica

Questions or Comments? 877.746.4407, Mon-Fri 8A.M.-6P.M. EST

See outer box for all Drug Facts

Front View Box

Colorlogix ®

Clear and Sheer

Broad Spectrum SPF 50

100% mineral based foundation + sunscreen


AM ALL SKIN TYPES

0.19 OZ | 5.5G

Box

Front View Tube

Colorlogix ®

Clear and Sheer

Broad Spectrum SPF 50

100% mineral based foundation + sunscreen


AM ALL SKIN TYPES

0.19 OZ | 5.5G

Tube

COLORLOGIX CLEAR AND SHEER 
it clear powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 81846-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE250 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MICA (UNII: V8A1AW0880)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 81846-001-015.5 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product03/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/01/2020
Labeler - Induction Therapies LLC (098256562)
Establishment
NameAddressID/FEIBusiness Operations
Induction Therapies, LLC098256562label(81846-001)

Revised: 5/2023