NEXICLEAR ACNE TREATMENT- salicylic acid liquid

NEXICLEAR ACNE TREATMENT by

Drug Labeling and Warnings

NEXICLEAR ACNE TREATMENT by is a Otc medication manufactured, distributed, or labeled by Results RNA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NEXICLEAR ACNE TREATMENT

ACTIVE INGREDIENT

Salicylic Acid 2%

PURPOSE

Acne Treatment

USES

For the treatment of acne

WARNINGS

For external use only

• Avoid eyebrows and hairline as product may lighten hair color
  

When using this product

• 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.
  

KEEP OUT OF REACH OF CHILDREN

DIRECTIONS

• Clean skin thoroughly before applying this product
• Wipe affected area with activated pad one to three time daily, if needed, or as directed by a doctor.
• If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
  

OTHER INFORMATION

• Store in a cool dry place
• Close jar tightly
  

INACTIVE INGREDIENTS

Distilled Water,  Green Tea Leaf, Soapwort Herb, Agrimony Herb, Marigold Flower Petals, Oregon Grape Root, Glycerin, Hydrogen Peroxide, Phenethyl Alcohol

Questions?

Call: 1 888 823 3869

ACTIVATE BEFORE USE

Step 1: Remove one moistened pad from the main jar and place pad inside jar lid.

Step 2: To activate pad, moisten pad further with 10 sprays of Activator solution.

Step 3: Using Activated pad, cover affected skin areas with wiping motion. Repeat until pad moisture is used.

Step 4: Allow formula to fry and remain on skin. Do not rinse off.

Results RNA

www.nexiclear.com

Orem, Utah 84058

Made in USA

Patent Pending

Satisfaction Guaranteed

1 888 823 3869

NEXICLEAR Acne Treatment 60 pads (

42876-002-60)

NEXICLEAR
PROFESSIONAL SKIN CARE

ACNE TREATMENT

60 MEDICATED PADS

INGREDIENTS AND APPEARANCE

NEXICLEAR ACNE TREATMENT 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42876-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
SAPONARIA OFFICINALIS WHOLE (UNII: 4V1PP5J0HJ)
AGRIMONIA EUPATORIA (UNII: EBU0U94820)
CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
MAHONIA AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42876-002-60	60 in 1 JAR
1		3.2 mL in 1 PATCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	02/29/2012

Labeler - Results RNA, LLC (078395000)

Registrant - Results RNA, LLC (078395000)

Establishment
Name	Address	ID/FEI	Business Operations
Results RNA, LLC		078395000	manufacture