Control Anti-Dandrudff description, usages, side effects, indications, overdosage, supplying and lots more!

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Control Anti-Dandrudff

AG Professional Hair Care Products, Ltd

Control Anti-Dandruff Shampoo


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT:

PURPOSE:

Anti-Dandruff

USES:

HELPS PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.

STOP USE AND ASK A DOCTOR IF

CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED.

KEEP THIS AND ALL DRUGS OUT OF REACH OF CHILDREN

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

  • USE TWICE A WEEK, OR AS DIRECTED BY A PHYSICIAN FOR CHRONIC CONDITIONS.
  • MASSAGE INTO SCALP FOR 3-5 MINUTES. RINSE THOROUGHLY.

INACTIVE INGREDIENTS

WATER/AQUA/EAU, AMMONIUM LAURETH SULFATE, TEA-LAURYL SULFATE, TRIETHANOLAMINE, LAURYL PYRROLIDONE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, PANTHENOL, SILK AMINO ACIDS, COCODIMONIUM HYDROXYPROPYL HYDROLYZED KERATIN, SODIUM PCA, TOCOPHERYL ACETATE, SODIUM HYDROXYMETHYLGLYCINATE, ETHYLHEXYL METHOXYCINNAMATE, CITRIC ACID, PARFUM/FRAGRANCE, MENTHOL, PROPYLENE GLYCOL, DIAZOLIDINYL UREA, IODOPROPYNYL BUTYLCARBAMATE, YELLOW 5 (CI 19140), RED 33 (CI 17200).

QUESTIONS (OR COMMENTS)?

1-866-924-4247

aghair.com
®/TM are/sont
REG TM OF MD/de
PO BOX 57045 VANCOUVER
BC CANADA V5K 5G6
Made in/
fabriqué au Canada
0611

PRODUCT LABELING







Control Anti-Dandrudff

Control Anti-Dandrudff

PYRITHIONE ZINC SHAMPOO

Product Information

Product Type Human otc drug label Item Code (Source) NDC:46324-2421
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC 2 mL

Inactive Ingredients

Ingredient Name Strength
water
trolamine lauryl sulfate
TROLAMINE
Lauryl Pyrrolidone
PANTHENOL
SODIUM PYRROLIDONE CARBOXYLATE
ALPHA-TOCOPHEROL ACETATE
SODIUM HYDROXYMETHYLGLYCINATE
OCTINOXATE
CITRIC ACID MONOHYDRATE
MENTHOL
propylene glycol
DIAZOLIDINYL UREA
IODOPROPYNYL BUTYLCARBAMATE
FD&C YELLOW NO. 5
D&C RED NO. 33

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:46324-2421-8 237 in 1 BOTTLE
2 NDC:46324-2421-1 1000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2011-10-28


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