SAFEWAY DANDRUFF DRY SCALP- pyrithione zinc shampoo

Nazione: Stati Uniti

Lingua: inglese

Fonte: NLM (National Library of Medicine)

Principio attivo:

PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)

Commercializzato da:

SAFEWAY INC.

INN (Nome Internazionale):

PYRITHIONE ZINC

Composizione:

PYRITHIONE ZINC 1.0 mL in 100 mL

Via di somministrazione:

TOPICAL

Tipo di ricetta:

OTC DRUG

Indicazioni terapeutiche:

TO HELP PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF.

Stato dell'autorizzazione:

OTC monograph final

Scheda tecnica

SAFEWAY DANDRUFF DRY SCALP- PYRITHIONE ZINC SHAMPOO
SAFEWAY INC.
_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._
----------
DRUG FACTS
ACTIVE INGREDIENT
PYRITHIONE ZINC 1%
PURPOSE
ANTIDANDRUFF
USES
TO HELP 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 WITH WATER.
STOP USING THIS PRODUCT AND ASK DOCTOR IF
CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS
PRODUCT
AS DIRECTED.
KEEP OUT OF REACH OF CHILDREN
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON
CONTROL CENTER IMMEDIATELY.
DIRECTIONS
FOR MAXIMUM DANDRUFF CONTROL, USE EVERY TIME YOU SHAMPOO. WET HAIR,
MASSAGE ONTO SCALP AND RINSE. REPEAT IF DESIRED.
INACTIVE INGREDIENTS:
WATER (AQUA), SODIUM LAURETH SULFATE, SODIUM LAURYL SULFATE, COCAMIDE
MEA, ZINC CARBONATE, GLYCOL DISTEARATE, DIMETHICONE, FRAGRANCE
(PARFUM),
CETYL ALCOHOL, POLYQUATERNIUM-10, MAGNESIUM SULFATE, SODIUM BENZOATE,
MAGNESIUM CARBONATE HYDROXIDE, AMMONIUM LAURETH SULFATE, BENZYL
ALCOHOL, SODIUM CHLORIDE, METHYLCHLOROISOTHIAZOLINONE,
METHYLISOTHIAZOLINONE, SODIUM XYLENESULFONATE.
QUESTIONS OR COMMENTS?
1-888-723-3929
LABEL COPY
SAFEWAY DANDRUFF DRY SCALP
pyrithione zinc shampoo
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:21130 -416
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
PYRITHIO NE ZINC (UNII: R9 53O2RHZ5) (PYRITHIONE ZINC - UNII:R9
53O2RHZ5)
PYRITHIONE ZINC
1.0 mL in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
SO DIUM LAURETH SULFATE (UNII: BPV39 0 UAP0 )
SO DIUM LAURYL SULFATE (UNII: 36 8 GB5141J)
CO CO MO NO ETHANO LAMIDE (UNII: C8 0 6 8 4146 D)
ZINC CARBO NATE (UNII: EQR32Y7H0 M)
GLYCO L DISTEARATE (UNII: 13W7MDN21W)
DIMETHICO NE (UNII: