Label: IASO CONTROL MAKE UP BASE 60- zinc oxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 75847-1712-1 - Packager: IASO Inc
- 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 March 2, 2018
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
water, cyclopentasiloxane, ethylhexyl methoxycinnamate, glycerin, ethylhexyl salicylate, peg-10 dimethicone, dipropylene glycol, cyclomethicone, betaine, disteardimonium hectorite, hexyl laurate, magnesium sulfate, talc, aluminum hydroxide, aluminum stearate, methylparaben palmitic acid, acrylates/dimethicone copolymer, fragrance, imidazolidinyl urea, chromium, oxide greens, dimethicone/vinyl dimethicone crosspolymer, methicone, propylparaben, silica, tocopheryl acetate, butylparaben, distearyldimonium chloride, glycosyl trehalose, hydrogenated starch hydrolysate, dimethicone, ci 77492, aloe barbadensis leaf juice, bisabolol, camellia sinensis leaf extract, hydrolyzed lupine protein, morus nigra leaf ext, panax ginseng root ext, squalane, portulaca oleracea extract, rosa canina fruit oil, rosa centifolia flower water, rosemary leaf ext, stearyl glycyrrhetinate
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
IASO CONTROL MAKE UP BASE 60
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75847-1712 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.03 g in 1 mL Inactive Ingredients Ingredient Name Strength DIMETHICONE (UNII: 92RU3N3Y1O) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) CYCLOMETHICONE (UNII: NMQ347994Z) SQUALENE (UNII: 7QWM220FJH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75847-1712-1 35 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/12/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 08/01/2013 Labeler - IASO Inc (688771690) Registrant - IASO Inc (688771690) Establishment Name Address ID/FEI Business Operations Kolmar Korea Co., Ltd 689512611 manufacture(75847-1712)