Package 87093-114-75

Brand: lumiste invisible man

Generic: antiperspirant roll on
NDC Package

Package Facts

Identity

Package NDC 87093-114-75
Digits Only 8709311475
Product NDC 87093-114
Description

75 mL in 1 BOTTLE (87093-114-75)

Marketing

Marketing Status
Marketed Since 2025-12-01
Brand lumiste invisible man
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": "432f7e85-29fb-1b11-e063-6394a90a130d", "openfda": {"unii": ["HPN8MZW13M"], "spl_set_id": ["432f4a21-e326-e178-e063-6394a90ad231"], "manufacturer_name": ["COCO COSMETICS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (87093-114-75)", "package_ndc": "87093-114-75", "marketing_start_date": "20251201"}], "brand_name": "LUMISTE INVISIBLE MAN", "product_id": "87093-114_432f7e85-29fb-1b11-e063-6394a90a130d", "dosage_form": "LIQUID", "product_ndc": "87093-114", "generic_name": "ANTIPERSPIRANT ROLL ON", "labeler_name": "COCO COSMETICS INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LUMISTE INVISIBLE MAN", "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"}