Label: HAIRITAGE WASH IT AWAY ANTI-DANDRUFF FOR DRY, FLAKY SCALP- selenium sulfide liquid
- NDC Code(s): 71899-068-01
- Packager: Maesa, LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
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Warnings
- For external use only.
- Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
- Stop use and consult a doctor if condition worsens or does not improve after regular use of this product as directed.
- If condition covers a large area of the body, consult your doctor before using this product.
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Directions
- Shake well before each use.
- Apply to wet hair and massage, from scalp to ends. Rinse thoroughly and follow with Hairitage Balancing Conditioner. Substitute Hairitage Anti-Dandruff Shampoo with your regular shampoo every other wash, or when you notice dry and/or flaky scalp.
- For best results use at least twice a week or as directed by a doctor.
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Inactive Ingredients
WATER (AQUA/EAU), AMMONIUM LAURYL SULFATE, AMMONIUM LAURETH SULFATE, DISTEARYL PHTHALIC ACIDE AMIDE, COCAMIDE MEA, PHENOXYETHANOL, FRAGRANCE (PARFUM), HYDROXYPROPYL METHYLCELLULOSE, SODIUM CITRATE, CAPRYLYL GLYCOL, SODIUM LAUROYL LACTYLATE, SODIUM CHLORIDE, CITRIC ACID, C10-16 ALCOHOLS, AMMONIUM SULFATE, MAGNESIUM CHLORIDE, ALOE BARBADENSIS LEAF JUICE, TETRASODIUM, METHYLCHLOROISOTHIAZOLINONE, AMMONIUM CHLORIDE, METHYLISOTHIAZOLINONE, TRISODIUM NTA, TITANIUM DIOXIDE (CI 77891), BLUE 1 LAKE (CI 42090), YELLOW 10 (CI 47005), EXT. VIOLET 2 (CI 60730).
- Questions or Comments
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 384 mL Bottle Label
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INGREDIENTS AND APPEARANCE
HAIRITAGE WASH IT AWAY ANTI-DANDRUFF FOR DRY, FLAKY SCALP
selenium sulfide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71899-068 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Selenium Sulfide (UNII: Z69D9E381Q) (Selenium Sulfide - UNII:Z69D9E381Q) Selenium Sulfide 0.1 g in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) AMMONIUM LAURETH-12 SULFATE (UNII: E1ZP93931S) Phenoxyethanol (UNII: HIE492ZZ3T) Caprylyl Glycol (UNII: 00YIU5438U) Ammonium Lauryl Sulfate (UNII: Q7AO2R1M0B) Ammonium Sulfate (UNII: SU46BAM238) Ammonium Chloride (UNII: 01Q9PC255D) EDETATE SODIUM (UNII: MP1J8420LU) Trisodium Nitrilotriacetate (UNII: E3C8R2M0XD) Methylchloroisothiazolinone (UNII: DEL7T5QRPN) Methylisothiazolinone (UNII: 229D0E1QFA) DISTEARYL PHTHALAMIC ACID (UNII: 5552GSZ9LI) COCO MONOETHANOLAMIDE (UNII: C80684146D) Titanium Dioxide (UNII: 15FIX9V2JP) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) Sodium Chloride (UNII: 451W47IQ8X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Sodium Lauroyl Lactylate (UNII: 7243K85WFO) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) Magnesium Chloride (UNII: 02F3473H9O) Magnesium Nitrate (UNII: 77CBG3UN78) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71899-068-01 384 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/06/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 04/06/2023 Labeler - Maesa, LLC. (144282311) Establishment Name Address ID/FEI Business Operations Garcoa 255106239 MANUFACTURE(71899-068)
