Label: TATTOO AFTER CARE A AND D- lanolin and petrolatum ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 67234-066-01 - Packager: Natureplex 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 6, 2018
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- ACTIVE INGREDIENT
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 42.5 g Tube Carton
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INGREDIENTS AND APPEARANCE
TATTOO AFTER CARE A AND D
lanolin and petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67234-066 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lanolin (UNII: 7EV65EAW6H) (Lanolin - UNII:7EV65EAW6H) Lanolin 0.15 mg in 1 g Petrolatum (UNII: 4T6H12BN9U) (Petrolatum - UNII:4T6H12BN9U) Petrolatum 0.53 mg in 1 g Inactive Ingredients Ingredient Name Strength WHITE WAX (UNII: 7G1J5DA97F) COD LIVER OIL (UNII: BBL281NWFG) MINERAL OIL (UNII: T5L8T28FGP) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67234-066-01 1 in 1 CARTON 06/15/2018 1 42.5 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 06/15/2018 Labeler - Natureplex LLC (062808196) Establishment Name Address ID/FEI Business Operations Natureplex LLC 062808196 MANUFACTURE(67234-066)