Package 13709-351-01
Brand: itch relief
Generic: itch relief gelPackage Facts
Identity
Package NDC
13709-351-01
Digits Only
1370935101
Product NDC
13709-351
Description
1 TUBE in 1 CARTON (13709-351-01) / 103.5 mL in 1 TUBE
Marketing
Marketing Status
Brand
itch relief
Generic
itch relief gel
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "44811828-c32f-17fc-e063-6294a90add48", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049880"], "spl_set_id": ["44811828-c32e-17fc-e063-6294a90add48"], "manufacturer_name": ["Neilmed Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (13709-351-01) / 103.5 mL in 1 TUBE", "package_ndc": "13709-351-01", "marketing_start_date": "20251126"}], "brand_name": "Itch Relief", "product_id": "13709-351_44811828-c32f-17fc-e063-6294a90add48", "dosage_form": "GEL", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "13709-351", "generic_name": "Itch Relief Gel", "labeler_name": "Neilmed Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Itch Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251126", "listing_expiration_date": "20261231"}