Package 87093-111-75

Brand: lumiste bravo

Generic: antiperspirant roll on
NDC Package

Package 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
Marketed Since 2025-12-01
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"}