Label: PLAN B ONE-STEP- levonorgestrel tablet
- NDC Code(s): 69536-146-19, 69536-162-88, 69536-162-99
- Packager: Foundation Consumer Healthcare LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated January 31, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
Sexually transmitted diseases (STDs) alert
This product does not protect against HIV/AIDS or other STDs
Ask a doctor or pharmacist before use if you are taking efavirenz (HIV medication) or rifampin (tuberculosis treatment) or medication for seizures (epilepsy). These medications may reduce the effectiveness of levonorgestrel.
- Directions
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1.5 mg Tablet Blister Pack Box - NDC 69536-162-88
- PRINCIPAL DISPLAY PANEL - 1.5 mg Tablet Blister Pack Box - NDC 69536-146-19
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INGREDIENTS AND APPEARANCE
PLAN B ONE-STEP
levonorgestrel tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69536-162 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LEVONORGESTREL (UNII: 5W7SIA7YZW) (LEVONORGESTREL - UNII:5W7SIA7YZW) LEVONORGESTREL 1.5 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, POTATO (UNII: 8I089SAH3T) MAGNESIUM STEARATE (UNII: 70097M6I30) TALC (UNII: 7SEV7J4R1U) STARCH, CORN (UNII: O8232NY3SJ) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) Product Characteristics Color WHITE Score no score Shape ROUND Size 8mm Flavor Imprint Code G00 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69536-162-88 1 in 1 BOX, UNIT-DOSE 05/10/2018 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:69536-162-99 1 in 1 BOX, UNIT-DOSE 08/15/2019 2 1 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021998 05/10/2018 PLAN B ONE-STEP
levonorgestrel tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69536-146 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LEVONORGESTREL (UNII: 5W7SIA7YZW) (LEVONORGESTREL - UNII:5W7SIA7YZW) LEVONORGESTREL 1.5 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, POTATO (UNII: 8I089SAH3T) MAGNESIUM STEARATE (UNII: 70097M6I30) TALC (UNII: 7SEV7J4R1U) STARCH, CORN (UNII: O8232NY3SJ) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) Product Characteristics Color WHITE Score no score Shape ROUND Size 8mm Flavor Imprint Code G00 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69536-146-19 1 in 1 BOX, UNIT-DOSE 05/10/2018 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021998 05/10/2018 Labeler - Foundation Consumer Healthcare LLC (079675882)