Label: ROYAL DANDRUFF DRY SCALP- pyrithione zinc shampoo
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Contains inactivated NDC Code(s)
NDC Code(s): 73597-009-10 - Packager: Mission Series Inc. dba Prestige Beauty Care
- 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 May 18, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop Use
- Keep out of reach of children
- Directions
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Inactive Ingredients
Inactive Ingredients - Water, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Amodimethicone, Sodium Chloride, Glycol Distearate, Cetyl Alcohol, Cocamide MEA, Fragrance, Polyquaternium-10, Sodium Citrate, Hydrogentated Polydecene, Sodium Benzoate, Trideceth-12, Cetrimonium Chloride, Citric Acid, Ammonium Xylenesulfonate, FD&C Blue No. 1, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone.
- Distributed By
- Royal Dandruff Shampoo Dry Scalp
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INGREDIENTS AND APPEARANCE
ROYAL DANDRUFF DRY SCALP
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73597-009 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 AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6) AMODIMETHICONE (800 CST) (UNII: 363Z2T48P7) POLYQUATERNIUM-10 (10000 MPA.S AT 2%) (UNII: PI1STR9QYH) SODIUM CITRATE (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) TRIDECETH-12 (UNII: YFY3KG5Y7O) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) BENZYL ALCOHOL (UNII: LKG8494WBH) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) HYDROGENATED POLYDECENE TYPE I (UNII: U333RI6EB7) SODIUM CHLORIDE (UNII: 451W47IQ8X) CETYL ALCOHOL (UNII: 936JST6JCN) COCO MONOETHANOLAMIDE (UNII: C80684146D) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) GLYCOL DISTEARATE (UNII: 13W7MDN21W) AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73597-009-10 273.06 g in 1 BOTTLE; Type 0: Not a Combination Product 05/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 05/18/2020 Labeler - Mission Series Inc. dba Prestige Beauty Care (117190866)