Package 10738-051-10

Brand: nasal dryness relief gel

Generic: allantoin
NDC Package

Package Facts

Identity

Package NDC 10738-051-10
Digits Only 1073805110
Product NDC 10738-051
Product ID 10738-051_49655e27-0a67-4fca-e063-6294a90a5cfa
Description

1 TUBE in 1 CARTON (10738-051-10) / 28 g in 1 TUBE (10738-051-15)

Marketing

Marketing Status
Marketed Since 2022-05-20
Brand nasal dryness relief gel
Generic allantoin
Sample Package No

Linked Drug Pages (1)

Nasal Dryness Relief Gel ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "49655e27-0a67-4fca-e063-6294a90a5cfa", "openfda": {"unii": ["344S277G0Z"], "spl_set_id": ["dfece059-57bd-8eee-e053-2a95a90a980e"], "manufacturer_name": ["Genuine Virgin Aloe Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (10738-051-10)  / 28 g in 1 TUBE (10738-051-15)", "package_ndc": "10738-051-10", "marketing_start_date": "20220520"}], "brand_name": "Nasal Dryness Relief Gel", "product_id": "10738-051_49655e27-0a67-4fca-e063-6294a90a5cfa", "dosage_form": "GEL", "product_ndc": "10738-051", "generic_name": "Allantoin", "labeler_name": "Genuine Virgin Aloe Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nasal Dryness Relief Gel", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".5 g/100g"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220520", "listing_expiration_date": "20271231"}