lumiste night wood

Generic: antiperspirant roll on

Labeler: coco cosmetics inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name lumiste night wood
Generic Name antiperspirant roll on
Labeler coco cosmetics inc
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

aluminum chlorohydrate 12 mg/100mL

Manufacturer
COCO COSMETICS INC

Identifiers & Regulatory

Product NDC 87093-116
Product ID 87093-116_432f4a28-11f5-dc70-e063-6394a90a3e03
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 87093116
Hyphenated Format 87093-116

Supplemental Identifiers

UNII
HPN8MZW13M

Packaging Origin

Original Packager
true

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 night wood (source: ndc)
Generic Name antiperspirant roll on (source: ndc)
Application Number M019 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 12 mg/100mL
source: ndc
Packaging
  • 75 mL in 1 BOTTLE (87093-116-75)
source: ndc

Packages (1)

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

Ingredients (1)

aluminum chlorohydrate (12 mg/100mL)

Linked Drug Pages (1)

LUMISTE NIGHT WOOD ndc-match (0.9)

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"}