Label: SELENIUM SULFIDE shampoo
- NDC Code(s): 42582-900-06
- Packager: Bi-Coastal Pharma International LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Updated March 2, 2020
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- SPL UNCLASSIFIED SECTION
A liquid antiseborrehic, antifungal preparation for topical application.
Each mL of Selenium Sulfide 2.25% Shampoo contains 22.5 mg selenium sulfide, ammonium lauryl sulfate, caprylic/capric triglyceride, chromium oxide green, citric acid, cocamidopropyl betaine, D&C yellow #8, diazolidinyl urea, edetate disodium, FD&C red #40, fragrance, hydroxypropyl methylcellulose, magnesium aluminum silicate, methylparaben, panthenol, PPG-2 hydroxyethyl coco/isostearamide, propylene glycol, propylparaben, purified water, sodium citrate, titanium dioxide, tocopheryl acetate, urea, zinc pyrithione.
- CLINICAL PHARMACOLOGY
- INDICATIONS & USAGE
This medication is to be used as directed by a physician. Not to be used when inflammation or exudation is present as increased absorption may occur.
Dermal application of 25% and 50% solutions of 2.5% selenium sulfide lotion on mice over an 88-week period indicated no carcinogenic effects.
USE IN PREGNANCY
Animal reproduction studies have not been conducted with this medication. It is also not known whether this product can cause fetal harm when applied to the body surfaces of a pregnant woman or can affect reproduction capacity. Under ordinary circumstances, selenium sulfide 2.25% shampoo should not be used by pregnant women.
It is not known whether or not this drug is secreted in human milk. Because many drugs are secreted in human milk, caution should be exercised when this product is administered to a nursing woman.
- ADVERSE REACTIONS
There are no documented reports of serious toxicity in humans resulting from acute ingestion of selenium sulfide 2.25% shampoo. However, acute toxicity studies in animals suggest that ingestion of large amounts could result in potential human toxicity. Evacuation of the stomach contents should be considered in cases of acute oral ingestion.
DOSAGE AND ADMINISTRATION
SHAKE WELL BEFORE USING
For seborrheic dermatitis and dandruff
Generally 2 applications each week for 2 weeks will control symptoms. Subsequently, shampoo may be used less frequently – weekly, every 2 weeks, every 3 to 4 weeks or as directed by a physician. Should not be applied more frequently than necessary to maintain control.
Selenium Sulfide 2.25% Shampoo is supplied in 180 mL bottles, NDC 42582-900-06.
Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C and 30°C (between 59°F and 86°F). Brief exposure to temperatures up to 40°C (104°F) may be tolerated provided the mean kinetic temperature does not exceed 25°C (77°F); however, such exposure should be minimized. Protect from freezing.
KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 180 mL Bottle Carton
INGREDIENTS AND APPEARANCE
selenium sulfide shampoo
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:42582-900 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Selenium Sulfide (UNII: Z69D9E381Q) (Selenium Sulfide - UNII:Z69D9E381Q) Selenium Sulfide 22.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength ammonium lauryl sulfate (UNII: Q7AO2R1M0B) medium-chain triglycerides (UNII: C9H2L21V7U) chromic oxide (UNII: X5Z09SU859) citric acid monohydrate (UNII: 2968PHW8QP) cocamidopropyl betaine (UNII: 5OCF3O11KX) fluorescein sodium (UNII: 93X55PE38X) diazolidinyl urea (UNII: H5RIZ3MPW4) edetate disodium (UNII: 7FLD91C86K) FD&C red no. 40 (UNII: WZB9127XOA) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) magnesium aluminum silicate (UNII: 6M3P64V0NC) methylparaben (UNII: A2I8C7HI9T) panthenol (UNII: WV9CM0O67Z) PPG-2 hydroxyethyl coco/isostearamide (UNII: EK4J71ZKEQ) propylene glycol (UNII: 6DC9Q167V3) propylparaben (UNII: Z8IX2SC1OH) water (UNII: 059QF0KO0R) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) titanium dioxide (UNII: 15FIX9V2JP) .alpha.-tocopherol acetate (UNII: 9E8X80D2L0) urea (UNII: 8W8T17847W) pyrithione zinc (UNII: R953O2RHZ5) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42582-900-06 1 in 1 CARTON 06/01/2011 1 180 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 06/01/2011 Labeler - Bi-Coastal Pharma International LLC (078397428)