up and up nicotine mini mint

Generic: nicotine polacrilex

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name up and up nicotine mini mint
Generic Name nicotine polacrilex
Labeler target corporation
Dosage Form LOZENGE
Routes
ORAL
Active Ingredients

nicotine 4 mg/1

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 82442-957
Product ID 82442-957_31a27d29-0833-4e84-85be-321513ec2b65
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA203690
Listing Expiration 2026-12-31
Marketing Start 2024-05-17

Pharmacologic Class

Established (EPC)
cholinergic nicotinic agonist [epc]
Chemical Structure
nicotine [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82442957
Hyphenated Format 82442-957

Supplemental Identifiers

RxCUI
359818
UPC
0012345678905
UNII
6M3C89ZY6R
NUI
N0000175706 M0014836

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name up and up nicotine mini mint (source: ndc)
Generic Name nicotine polacrilex (source: ndc)
Application Number ANDA203690 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 3 CONTAINER in 1 CARTON (82442-957-03) / 27 LOZENGE in 1 CONTAINER (82442-957-01)
  • 1 CONTAINER in 1 CARTON (82442-957-60) / 20 LOZENGE in 1 CONTAINER
source: ndc

Packages (2)

Ingredients (1)

nicotine (4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31a27d29-0833-4e84-85be-321513ec2b65", "openfda": {"nui": ["N0000175706", "M0014836"], "upc": ["0012345678905"], "unii": ["6M3C89ZY6R"], "rxcui": ["359818"], "spl_set_id": ["43f9d241-3af1-46cb-abe9-8c25427472aa"], "pharm_class_cs": ["Nicotine [CS]"], "pharm_class_epc": ["Cholinergic Nicotinic Agonist [EPC]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 CONTAINER in 1 CARTON (82442-957-03)  / 27 LOZENGE in 1 CONTAINER (82442-957-01)", "package_ndc": "82442-957-03", "marketing_start_date": "20240517"}, {"sample": false, "description": "1 CONTAINER in 1 CARTON (82442-957-60)  / 20 LOZENGE in 1 CONTAINER", "package_ndc": "82442-957-60", "marketing_start_date": "20240517"}], "brand_name": "up and up nicotine mini mint", "product_id": "82442-957_31a27d29-0833-4e84-85be-321513ec2b65", "dosage_form": "LOZENGE", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "82442-957", "generic_name": "Nicotine Polacrilex", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up nicotine mini mint", "active_ingredients": [{"name": "NICOTINE", "strength": "4 mg/1"}], "application_number": "ANDA203690", "marketing_category": "ANDA", "marketing_start_date": "20240517", "listing_expiration_date": "20261231"}