Denorex Extra Strength description, usages, side effects, indications, overdosage, supplying and lots more!

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Denorex Extra Strength

Ultimark Products LLC

Denorex Extra Strength




FULL PRESCRIBING INFORMATION

Drug Facts

Salicylic acid 3%

Controls the symptoms of dandruff, seborrheic dermatitis and psoriasis

  • Reduces and helps eliminate scalp itching, flaking and scaling associated with dandruff, seborrheic dermatitis and psoriasis
  • Helps prevent recurrence of the symptoms of dandruff, seborrheic dermatitis and psoriasis

For external use only.

a condition that covers a large area of the body.

avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

condition worsens or does not improve after regular use of this product as directed.

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

  • Shake well
  • apply to wet hair
  • gently massage into hair and scalp to work up a lather
  • rinse thoroughly and repeat
  • for best results, use at least twice weekly or as directed by a doctor

Store at 20º-25º C (68º – 77º F)

cocamidopropyl betaine, D&C Red No. 33, D&C Yellow No. 10, dimethicone PEG-8 meadowfoamate, FD&C Blue No. 1, FD&C Yellow No. 6, fragrance, glycol distearate, menthol, panthenol, polyquaternium-10, PPG-2 hydroxyethyl cocamide, propylene glycol, sodium C14-C16 olefin sulfonate, sodium citrate, vitamin E acetate, water

1-800-220-0151

www.denorex.net

EXTRA STRENGTH DENOREX
3 % Salicylic Acid

DANDRUFF
Control
SHAMPOO +

CONDITIONER

10 FL OZ (296
mL)

Denorex Extra Strength

Denorex Extra Strength

Salicylic Acid SHAMPOO

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51545-210
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Salicylic Acid SALICYLIC ACID 0.03 g

Inactive Ingredients

Ingredient Name Strength
water
SODIUM C14-16 OLEFIN SULFONATE
propylene glycol
GLYCOL DISTEARATE
MENTHOL
COCAMIDOPROPYL BETAINE
PANTHENOL
.ALPHA.-TOCOPHEROL ACETATE
SODIUM CITRATE
FD&C YELLOW NO. 6
D&C YELLOW NO. 10
D&C RED NO. 33
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51545-210-12 296 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2009-11-01


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Be sure to consult your doctor before taking any medication!
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