Label: RITE AID DANDRUFF 2 IN 1 DRY SCALP CARE- pyrithione zinc shampoo
-
Contains inactivated NDC Code(s)
NDC Code(s): 11822-4111-5 - Packager: Rite Aid Corporation
- 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 October 20, 2010
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Directions
-
Inactive Ingredients
Water, Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamide MEA, Glycol Distearate, Dimethicone, Zinc Carbonate, Fragrance, Cetyl Alcohol, Polyquaternium-10, Magnesium Sulfate, Sodium Benzoate, Magnesium Carbonate Hydroxide, Ammonium Laureth Sulfate, Benzyl Alcohol, Sodium Chloride, Elaeis Guineensis (Palm) Oil, Sodium Xylenesulfonate, Aloe Barbadensis Leaf, Anthemis Nobilis Flower Oil, Tocopheryl Acetate, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 10
- Principle Display Panel
-
INGREDIENTS AND APPEARANCE
RITE AID DANDRUFF 2 IN 1 DRY SCALP CARE
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-4111 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 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM LAURYL SULFATE (UNII: 368GB5141J) COCO MONOETHANOLAMIDE (UNII: C80684146D) GLYCOL DISTEARATE (UNII: 13W7MDN21W) DIMETHICONE (UNII: 92RU3N3Y1O) ZINC CARBONATE (UNII: EQR32Y7H0M) CETYL ALCOHOL (UNII: 936JST6JCN) MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I) SODIUM BENZOATE (UNII: OJ245FE5EU) ALMAGATE (UNII: 568Z59H7ZJ) AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6) BENZYL ALCOHOL (UNII: LKG8494WBH) SODIUM CHLORIDE (UNII: 451W47IQ8X) PALM OIL (UNII: 5QUO05548Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-4111-5 449 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 10/20/2010 Labeler - Rite Aid Corporation (014578892) Registrant - Apollo Health and Beauty Care (201901209) Establishment Name Address ID/FEI Business Operations Apollo Health and Beauty Care 201901209 manufacture