OTC Labels

Over the Counter Medications

OTC Medication Information: KANDESN DANDRUFF

KANDESN DANDRUFF — salicylic acid shampoo
Sunrider Manufacturing L.P.

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.

Directions

  • Apply small amount to wet hair , massage gently, then rinse thoroughly,
  • If desired, apply conditioner throughout hair; then rinse thoroughly.
  • For best results, use at least twice a week or as directed by a doctor.

Active Ingredient:

Salicylic Acid 2.8%

Water (Deionized)

KEEP OUT OF THE REACT OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away.

Antidandruff

Warnings:
  • For external use only
  • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Consult a doctor if conditions worsen or do not improve after regular use of this product as directed.

Controls the symptoms of dandruff


Shampoo

image of bottle label
(click image for full-size original)

Use: Controls the symptoms of dandruff.

KANDESN DANDRUFF
salicylic acid shampoo
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62191-006
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Salicylic Acid (Salicylic Acid) Salicylic Acid 28 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
SODIUM LAUROYL SARCOSINATE
COCAMIDOPROPYL BETAINE
LAURIC DIETHANOLAMIDE
GLYCOL DISTEARATE
DIETHYLENE GLYCOL MONOETHYL ETHER
COCO GLUCOSIDE
RICE GERM
SODIUM CITRATE
SODIUM CITRATE
SALIX ALBA BARK
ZINC PIDOLATE
ROSEMARY
CYMBOPOGON SCHOENANTHUS LEAF
HYPROMELLOSE 2208 (4000 MPA.S)
MAGNESIUM ALUMINUM SILICATE
MATRICARIA RECUTITA
EDETATE DISODIUM
POTASSIUM HYDROXIDE
CYSTEINE
METHIONINE
PYRIDOXINE
TEA TREE OIL
PYRITHIONE ZINC
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62191-006-01 120 g in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358H 03/01/2002
Labeler — Sunrider Manufacturing L.P. (786951475)
Registrant — Sunrider Manufacturing L.P. (786951475)

Revised: 02/2012 Sunrider Manufacturing L.P.