VIE NATURELLE ACNE BODY- benzoyl peroxide liquid

VIE NATURELLE ACNE BODY by

Drug Labeling and Warnings

VIE NATURELLE ACNE BODY by is a Otc medication manufactured, distributed, or labeled by TNT PRO SERIES. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS:

Active Ingredients:

Benzoyl Peroxide 2.5%

Acne Treatment

Use For:

For the treatment of acne. Clears up acne pimples and blemishes, and allows skin to heal. Helps prevent new pimples and blemishes from forming.

Warnings:

• For external use only.
• Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin.
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor. If bothersome dryness or peeling occurs, reduce application to once per day.

Do not use

for prolonged periods without consulting a doctor.

Keep out of reach of children.

If swallowed, contact physician or poison control center immediately. Store at room temperature.

Directions:

Cleanse the skin thoroughly before applying medication. Apply an even layer over affected area. Do not use on broken skin or large parts of the body. *For best results apply one to three times per day.

Other Ingredients:

Aqua (Deionized Water), Ethylhexylglycerin, Eucalyptus Globulus Oil, Hamamelis Virginiana (Witch Hazel) Distillate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer Melaleuca Alternifolia (Tea Tree) Oil, Phenoxyethanol, Polysorbate-20, Salicylic Acid.

Package Labeling:

INGREDIENTS AND APPEARANCE

VIE NATURELLE ACNE BODY 
benzoyl peroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73350-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	25 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
EUCALYPTUS OIL (UNII: 2R04ONI662)
WITCH HAZEL (UNII: 101I4J0U34)
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SALICYLIC ACID (UNII: O414PZ4LPZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73350-105-08	237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/05/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	08/05/2019

Labeler - TNT PRO SERIES (080998718)