lumiste invisible man
Generic: antiperspirant roll on
Labeler: coco cosmetics incDrug Facts
Product Profile
Brand Name
lumiste invisible man
Generic Name
antiperspirant roll on
Labeler
coco cosmetics inc
Dosage Form
LIQUID
Routes
Active Ingredients
aluminum chlorohydrate 12 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
87093-114
Product ID
87093-114_432f7e85-29fb-1b11-e063-6394a90a130d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M019
Listing Expiration
2026-12-31
Marketing Start
2025-12-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
87093114
Hyphenated Format
87093-114
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lumiste invisible man (source: ndc)
Generic Name
antiperspirant roll on (source: ndc)
Application Number
M019 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12 mg/100mL
Packaging
- 75 mL in 1 BOTTLE (87093-114-75)
Packages (1)
Ingredients (1)
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"}