Package 52651-056-02
Brand: tn dickinsons pain and itch relief
Generic: pramoxine hydrochloride and zinc acetatePackage Facts
Identity
Package NDC
52651-056-02
Digits Only
5265105602
Product NDC
52651-056
Description
103.5 mL in 1 BOTTLE, PUMP (52651-056-02)
Marketing
Marketing Status
Brand
tn dickinsons pain and itch relief
Generic
pramoxine hydrochloride and zinc acetate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d816e720-1970-4a35-b90e-9a29e179f774", "openfda": {"unii": ["88AYB867L5", "FM5526K07A"], "spl_set_id": ["537c9c27-ee81-4920-8e3f-21edb844c9cf"], "manufacturer_name": ["Dickinson Brands Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "103.5 mL in 1 BOTTLE, PUMP (52651-056-02)", "package_ndc": "52651-056-02", "marketing_start_date": "20260203"}], "brand_name": "TN Dickinsons Pain and Itch Relief", "product_id": "52651-056_d816e720-1970-4a35-b90e-9a29e179f774", "dosage_form": "LIQUID", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "52651-056", "generic_name": "Pramoxine Hydrochloride and Zinc Acetate", "labeler_name": "Dickinson Brands Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TN Dickinsons Pain and Itch Relief", "active_ingredients": [{"name": "PRAMOXINE HYDROCHLORIDE", "strength": ".01 g/mL"}, {"name": "ZINC ACETATE", "strength": ".001 g/mL"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260203", "listing_expiration_date": "20271231"}