dawnmist antiperspirant
Generic: aluminum chlorohydrate
Labeler: dukal llcDrug Facts
Product Profile
Brand Name
dawnmist antiperspirant
Generic Name
aluminum chlorohydrate
Labeler
dukal llc
Dosage Form
LOTION
Routes
Active Ingredients
aluminum chlorohydrate 45 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65517-2032
Product ID
65517-2032_2969b490-0bb9-21fe-e063-6394a90a5f2e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M019
Listing Expiration
2026-12-31
Marketing Start
2024-08-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
655172032
Hyphenated Format
65517-2032
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
dawnmist antiperspirant (source: ndc)
Generic Name
aluminum chlorohydrate (source: ndc)
Application Number
M019 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 45 mg/mL
Packaging
- 59 mL in 1 BOTTLE (65517-2032-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2969b490-0bb9-21fe-e063-6394a90a5f2e", "openfda": {"unii": ["HPN8MZW13M"], "spl_set_id": ["1fbdd228-e26a-275b-e063-6394a90a4c2f"], "manufacturer_name": ["Dukal LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE (65517-2032-1)", "package_ndc": "65517-2032-1", "marketing_start_date": "20240830"}], "brand_name": "DawnMist Antiperspirant", "product_id": "65517-2032_2969b490-0bb9-21fe-e063-6394a90a5f2e", "dosage_form": "LOTION", "product_ndc": "65517-2032", "generic_name": "Aluminum Chlorohydrate", "labeler_name": "Dukal LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DawnMist Antiperspirant", "active_ingredients": [{"name": "ALUMINUM CHLOROHYDRATE", "strength": "45 mg/mL"}], "application_number": "M019", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240830", "listing_expiration_date": "20261231"}