Ulta Vanilla Sugar Anti-Bacterial Gentle Foaming description, usages, side effects, indications, overdosage, supplying and lots more!

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Ulta Vanilla Sugar Anti-Bacterial Gentle Foaming

Ulta
Willard Manufacturing Inc.

DRUG FACTS:




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient:                     Purpose 

Triclosan 0.3% .........................Antibacterial


Purpose

USE: 


Keep out of reach of children. If swallowed, get medical help

or contact a Poison Control Center right away.

Warnings

For external use only

_________________________________

When using this product do not use in or near the eyes.

If contact occurs, rinse thoroughly with water.

_________________________________

Discontinue use if irritation or redness develops.  If condition persists

for more than 72 hours, consult a doctor.

Uses

Directions - Lather onto moist skin - Massage and rinse well.




Inactive Ingredients

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Fragrance, Propylene Glycol,

Helianthus Annuus (Sunflower) Seed Oil, Polyquaternium-7, Tetrasodium EDTA,

Benzophenone-4, Mentha Piperita (Peppermint) Leaf Extract, Citrus Aurantium Dulcis

(Orange) Peel Extract, Avena Sativa (Oat) Kernel Extract, Tocopheryl Acetate,

Methylchloroisothiazolinone, Methylisothiazolinone, Red 40, Yellow 5


Ulta Vanilla Sugar Anti-Bacterial Gentle Foaming

Ulta Vanilla Sugar Anti-Bacterial Gentle Foaming

Triclosan LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62296-0021
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 0.3 g

Inactive Ingredients

Ingredient Name Strength
water
SODIUM LAURETH SULFATE
COCAMIDOPROPYL BETAINE
propylene glycol
SUNFLOWER OIL
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD)
EDETATE SODIUM
SULISOBENZONE
MENTHA PIPERITA LEAF
ORANGE PEEL
OAT
ALPHA-TOCOPHEROL ACETATE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE

Product Characteristics

Color
yellow (FD&C yellow no. 5)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62296-0021-1 242 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2011-06-15


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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