Package 87093-111-75
Brand: lumiste bravo
Generic: antiperspirant roll onPackage Facts
Identity
Package NDC
87093-111-75
Digits Only
8709311175
Product NDC
87093-111
Description
75 mL in 1 BOTTLE (87093-111-75)
Marketing
Marketing Status
Brand
lumiste bravo
Generic
antiperspirant roll on
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "432f54db-d174-aca1-e063-6294a90a34fe", "openfda": {"unii": ["HPN8MZW13M"], "spl_set_id": ["4030f559-1c9c-0d8b-e063-6294a90a6536"], "manufacturer_name": ["COCO COSMETICS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (87093-111-75)", "package_ndc": "87093-111-75", "marketing_start_date": "20251201"}], "brand_name": "LUMISTE BRAVO", "product_id": "87093-111_432f54db-d174-aca1-e063-6294a90a34fe", "dosage_form": "LIQUID", "product_ndc": "87093-111", "generic_name": "ANTIPERSPIRANT ROLL ON", "labeler_name": "COCO COSMETICS INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LUMISTE BRAVO", "active_ingredients": [{"name": "ALUMINUM CHLOROHYDRATE", "strength": "12 mg/100mL"}], "application_number": "M019", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}