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
- 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 10, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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 FINAL part358H 04/06/2023 Labeler - Maesa, LLC. (144282311) Establishment Name Address ID/FEI Business Operations Garcoa 255106239 MANUFACTURE(71899-068)
