Package 61734-021-03
Brand: blue ice analgesic
Generic: mentholPackage Facts
Identity
Package NDC
61734-021-03
Digits Only
6173402103
Product NDC
61734-021
Description
227 g in 1 CONTAINER (61734-021-03)
Marketing
Marketing Status
Brand
blue ice analgesic
Generic
menthol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4148fe86-faf7-93a6-e063-6294a90ab4d8", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["311502"], "spl_set_id": ["184ed488-6e62-40c6-bb71-1d523280fd6b"], "manufacturer_name": ["Delon Laboratories (1990) Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 CONTAINER (61734-021-03)", "package_ndc": "61734-021-03", "marketing_start_date": "20100507"}], "brand_name": "Blue Ice Analgesic", "product_id": "61734-021_4148fe86-faf7-93a6-e063-6294a90ab4d8", "dosage_form": "GEL", "product_ndc": "61734-021", "generic_name": "Menthol", "labeler_name": "Delon Laboratories (1990) Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Blue Ice Analgesic", "active_ingredients": [{"name": "MENTHOL", "strength": "2 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100507", "listing_expiration_date": "20261231"}