Label: UP AND UP MULTI ACTION ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin b, pramoxine hcl ointment
- NDC Code(s): 11673-562-58
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2024
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- Active ingredients (in each gram)
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use if you have
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
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Package/Label Principal Display Panel
Compare to active ingredients in Neosporin® + Pain Itch Scar
pain itch scar
multi-action antibiotic ointment
first aid antibiotic/pain relieving ointment
bacitracin zinc/neomycin sulfate/polymyxin B sulfate/pramoxine HCl
long-lasting infection protection
powerful pain and itch relief for cuts, scrapes and burns
minimizes the appearance of scars
NET WT 0.5 OZ (14 g)
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INGREDIENTS AND APPEARANCE
UP AND UP MULTI ACTION ANTIBIOTIC
bacitracin zinc, neomycin sulfate, polymyxin b, pramoxine hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-562 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [USP'U] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 10000 [USP'U] in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength COCOA BUTTER (UNII: 512OYT1CRR) OLIVE OIL (UNII: 6UYK2W1W1E) PETROLATUM (UNII: 4T6H12BN9U) SODIUM PYRUVATE (UNII: POD38AIF08) COTTONSEED OIL (UNII: H3E878020N) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Product Characteristics Color YELLOW (Pale) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-562-58 1 in 1 CARTON 05/11/2017 04/30/2025 1 14 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 Drug M004 05/11/2017 04/30/2025 Labeler - Target Corporation (006961700)