Package 84724-0002-1
Brand: antiperspirant antisudorifique
Generic: antiperspirant antisudorifiquePackage Facts
Identity
Package NDC
84724-0002-1
Digits Only
8472400021
Product NDC
84724-0002
Description
62 mL in 1 BOTTLE (84724-0002-1)
Marketing
Marketing Status
Brand
antiperspirant antisudorifique
Generic
antiperspirant antisudorifique
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4615f4a1-641f-8d86-e063-6394a90a7c32", "openfda": {"upc": ["5025381000123"], "unii": ["3CYT62D3GA"], "spl_set_id": ["4615f436-a475-9178-e063-6394a90a70e9"], "manufacturer_name": ["Archifox GmbH & Co. KG"]}, "finished": true, "packaging": [{"sample": false, "description": "62 mL in 1 BOTTLE (84724-0002-1)", "package_ndc": "84724-0002-1", "marketing_start_date": "20251201"}], "brand_name": "ANTIPERSPIRANT ANTISUDORIFIQUE", "product_id": "84724-0002_4615f4a1-641f-8d86-e063-6394a90a7c32", "dosage_form": "SPRAY", "product_ndc": "84724-0002", "generic_name": "ANTIPERSPIRANT ANTISUDORIFIQUE", "labeler_name": "Archifox GmbH & Co. KG", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTIPERSPIRANT ANTISUDORIFIQUE", "active_ingredients": [{"name": "ALUMINUM CHLORIDE", "strength": "12.4 mg/62mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}