Package 69968-0223-1

Brand: benadryl extra strength itch stopping

Generic: diphenhydramine hydrochloride and zinc acetate
NDC Package

Package Facts

Identity

Package NDC 69968-0223-1
Digits Only 6996802231
Product NDC 69968-0223
Product ID 69968-0223_26b4b1f0-5cb0-7132-e063-6394a90a2c2f
Description

1 TUBE in 1 CARTON (69968-0223-1) / 28.3 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2009-11-01
Brand benadryl extra strength itch stopping
Generic diphenhydramine hydrochloride and zinc acetate
Sample Package No

Linked Drug Pages (3)

Benadryl Extra Strength Itch Stopping ndc-match (0.95) Johnson and Johnson All Purpose First Aid Kit ndc-match (0.95) Johnson and Johnson First Aid All Purpose 160 CT ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "26b4b1f0-5cb0-7132-e063-6394a90a2c2f", "openfda": {"upc": ["0312547171670"], "unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1087026", "1111764"], "spl_set_id": ["a1c1b878-d58f-41ff-b7a8-477f28c52667"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69968-0223-1)  / 28.3 g in 1 TUBE", "package_ndc": "69968-0223-1", "marketing_start_date": "20091101"}, {"sample": false, "description": "28.3 g in 1 TUBE (69968-0223-2)", "package_ndc": "69968-0223-2", "marketing_start_date": "20091101"}], "brand_name": "Benadryl Extra Strength Itch Stopping", "product_id": "69968-0223_26b4b1f0-5cb0-7132-e063-6394a90a2c2f", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69968-0223", "generic_name": "Diphenhydramine Hydrochloride and Zinc Acetate", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Extra Strength", "brand_name_suffix": "Itch Stopping", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/g"}, {"name": "ZINC ACETATE", "strength": "1 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20091101", "listing_expiration_date": "20261231"}