Label: MODESA 2 IN 1 DANDRUFF ALMOND OIL DRY SCALP- pyrithione zinc shampoo
-
Contains inactivated NDC Code(s)
NDC Code(s): 40104-432-01 - Packager: NINGBO PULISI DAILY CHEMICAL PRODUCTS CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 Label Information
Updated April 2, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
-
INACTIVE INGREDIENT
water, sodium laureth sulfate, sodium lauryl sulfate, glycol distearate, sodium chloride, zinc barbonate, sodium xylenesulfonate, amodimethicone, cocamidopropyl betaine, fragrance, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, citric acid, prunus amygdalus dulcis (sweet almond) oil, methylchloroisothiazolinone, methylisothiazolinone.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MODESA 2 IN 1 DANDRUFF ALMOND OIL DRY SCALP
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:40104-432 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 1 g in 100 g Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM CHLORIDE (UNII: 451W47IQ8X) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) ZINC SULFATE (UNII: 89DS0H96TB) DIMETHICONE (UNII: 92RU3N3Y1O) CETYL ALCOHOL (UNII: 936JST6JCN) BENZYL ALCOHOL (UNII: LKG8494WBH) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) SODIUM HYDROXIDE (UNII: 55X04QC32I) CITRIC ACID, 1-STEARYL ESTER (UNII: E945AJ51FA) SODIUM BENZOATE (UNII: OJ245FE5EU) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:40104-432-01 396.9 g in 1 PACKAGE; Type 0: Not a Combination Product 04/02/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 04/02/2019 Labeler - NINGBO PULISI DAILY CHEMICAL PRODUCTS CO., LTD. (529047265) Registrant - NINGBO PULISI DAILY CHEMICAL PRODUCTS CO., LTD. (529047265) Establishment Name Address ID/FEI Business Operations NINGBO PULISI DAILY CHEMICAL PRODUCTS CO., LTD. 529047265 manufacture(40104-432)