lume deodorant with clinical strength sweat control, soft powder

Generic: aluminum sesquichlorohydrate

Labeler: lume deodorant, llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name lume deodorant with clinical strength sweat control, soft powder
Generic Name aluminum sesquichlorohydrate
Labeler lume deodorant, llc.
Dosage Form STICK
Routes
TOPICAL
Active Ingredients

aluminum sesquichlorohydrate 2.46 g/14g

Manufacturer
Lume Deodorant, LLC.

Identifiers & Regulatory

Product NDC 84520-034
Product ID 84520-034_485c8837-f469-6d93-e063-6394a90a1dab
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M019
Listing Expiration 2027-12-31
Marketing Start 2025-12-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84520034
Hyphenated Format 84520-034

Supplemental Identifiers

UPC
0850068958375 0850074689423 0850042058725
UNII
UCN889409V

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 lume deodorant with clinical strength sweat control, soft powder (source: ndc)
Generic Name aluminum sesquichlorohydrate (source: ndc)
Application Number M019 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 2.46 g/14g
source: ndc
Packaging
  • 14 g in 1 CONTAINER (84520-034-01)
source: ndc

Packages (1)

84520-034-01 14 g in 1 CONTAINER (84520-034-01)

Ingredients (1)

aluminum sesquichlorohydrate (2.46 g/14g)

Linked Drug Pages (1)

Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Unscented, Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Clean Tangerine, Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Lavender Sage, Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Soft Powder, Lume Deodorant with Clinical Strength Sweat Control, Fresh Spring, Lume Deodorant with Clinical Strength Sweat Control, Vanilla Bliss, Lume Deodorant with Clinical Strength Sweat Control, Soft Powder ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "485c8837-f469-6d93-e063-6394a90a1dab", "openfda": {"upc": ["0850068958375", "0850074689423", "0850042058725"], "unii": ["UCN889409V"], "spl_set_id": ["1cebcddc-fa0f-8b73-e063-6394a90ab95e"], "manufacturer_name": ["Lume Deodorant, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 g in 1 CONTAINER (84520-034-01)", "package_ndc": "84520-034-01", "marketing_start_date": "20251222"}], "brand_name": "Lume Deodorant with Clinical Strength Sweat Control, Soft Powder", "product_id": "84520-034_485c8837-f469-6d93-e063-6394a90a1dab", "dosage_form": "STICK", "product_ndc": "84520-034", "generic_name": "Aluminum Sesquichlorohydrate", "labeler_name": "Lume Deodorant, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lume Deodorant with Clinical Strength Sweat Control, Soft Powder", "active_ingredients": [{"name": "ALUMINUM SESQUICHLOROHYDRATE", "strength": "2.46 g/14g"}], "application_number": "M019", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251222", "listing_expiration_date": "20271231"}