Package 69968-0242-3

Brand: benadryl extra strength itch stopping

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69968-0242-3
Digits Only 6996802423
Product NDC 69968-0242
Product ID 69968-0242_33854b34-d15c-96fa-e063-6394a90ac610
Description

103 mL in 1 TUBE (69968-0242-3)

Marketing

Marketing Status
Marketed Since 2013-10-01
Brand benadryl extra strength itch stopping
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Benadryl Extra Strength Itch Stopping ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "33854b34-d15c-96fa-e063-6394a90ac610", "openfda": {"upc": ["0312547171571"], "unii": ["TC2D6JAD40"], "rxcui": ["1049880", "1049882"], "spl_set_id": ["66a2fd60-1757-45cc-a195-ecb9241dca2a"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "103 mL in 1 TUBE (69968-0242-3)", "package_ndc": "69968-0242-3", "marketing_start_date": "20131001"}], "brand_name": "Benadryl Extra Strength Itch Stopping", "product_id": "69968-0242_33854b34-d15c-96fa-e063-6394a90ac610", "dosage_form": "GEL", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69968-0242", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Extra Strength Itch Stopping", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20131001", "listing_expiration_date": "20261231"}