Package 87093-116-75

Brand: lumiste night wood

Generic: antiperspirant roll on
NDC Package

Package Facts

Identity

Package NDC 87093-116-75
Digits Only 8709311675
Product NDC 87093-116
Product ID 87093-116_432f4a28-11f5-dc70-e063-6394a90a3e03
Description

75 mL in 1 BOTTLE (87093-116-75)

Marketing

Marketing Status
Marketed Since 2025-12-01
Brand lumiste night wood
Generic antiperspirant roll on
Sample Package No

Linked Drug Pages (1)

LUMISTE NIGHT WOOD ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "432f4a28-11f5-dc70-e063-6394a90a3e03", "openfda": {"unii": ["HPN8MZW13M"], "spl_set_id": ["432f4b22-7ffa-d4ef-e063-6394a90a2eac"], "manufacturer_name": ["COCO COSMETICS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (87093-116-75)", "package_ndc": "87093-116-75", "marketing_start_date": "20251201"}], "brand_name": "LUMISTE NIGHT WOOD", "product_id": "87093-116_432f4a28-11f5-dc70-e063-6394a90a3e03", "dosage_form": "LIQUID", "product_ndc": "87093-116", "generic_name": "ANTIPERSPIRANT ROLL ON", "labeler_name": "COCO COSMETICS INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LUMISTE NIGHT WOOD", "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"}