Label: MG217 PSORIASIS MEDICATED CONDITIONING- coal tar shampoo
- NDC Code(s): 68093-7232-1, 68093-7232-2
- Packager: Wisconsin Pharmacal Company
- 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 December 10, 2018
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only
When using this product
- avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
- use caution in exposing skin to sunlight. It may increase your tendency to sunburn for up to 24 hours after application.
- do not use with other forms of psoriasis therapy such as ultraviolet radiation or prescription drugs unless directed by a physician.
- do not use for prolonged periods without consulting a physician.
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients
Deionized Water, Sodium Lauryl Ether Sulfate, Cocamidopropyl Betaine, Lauramidopropyl Hydroxysultaine, Palmitic Betaine, Guar Hydroxypropyl-trimonium Chloride, Hydrolyzed Collagen, Phenoxyethanol, Methyl Paraben, n-Butyl Paraben, Ethyl Paraben, lsobutyl Paraben, Propyl Paraben, Fragrance, FD&C Blue #1 - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MG217 PSORIASIS MEDICATED CONDITIONING
coal tar shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68093-7232 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COAL TAR (UNII: R533ESO2EC) (COAL TAR - UNII:R533ESO2EC) COAL TAR 0.03 g in 1 g Inactive Ingredients Ingredient Name Strength PORK COLLAGEN (UNII: I8442U2G7J) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GUAR GUM (UNII: E89I1637KE) METHYLPARABEN (UNII: A2I8C7HI9T) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) BUTYLPARABEN (UNII: 3QPI1U3FV8) ETHYLPARABEN (UNII: 14255EXE39) LAURAMIDOPROPYL HYDROXYSULTAINE (UNII: VPE363894V) PROPYLPARABEN (UNII: Z8IX2SC1OH) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) PHENOXYETHANOL (UNII: HIE492ZZ3T) BETAINE (UNII: 3SCV180C9W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68093-7232-1 1 in 1 CARTON 03/01/2015 1 120 g in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:68093-7232-2 1 in 1 CARTON 03/01/2015 2 240 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 03/01/2015 Labeler - Wisconsin Pharmacal Company (800873986) Registrant - Wisconsin Pharmacal Company (800873986) Establishment Name Address ID/FEI Business Operations Wisconsin Pharmacal Company 800873986 manufacture(68093-7232)