ban roll-on antiperspirant deodorant satin breeze

Generic: aluminum chlorohydrate

Labeler: kao usa inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ban roll-on antiperspirant deodorant satin breeze
Generic Name aluminum chlorohydrate
Labeler kao usa inc.
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

aluminum chlorohydrate 20 g/103mL

Manufacturer
Kao USA Inc.

Identifiers & Regulatory

Product NDC 10596-339
Product ID 10596-339_21d9bd72-4a57-8024-e063-6394a90a1df8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M019
Listing Expiration 2026-12-31
Marketing Start 2012-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10596339
Hyphenated Format 10596-339

Supplemental Identifiers

UPC
0019045010080
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 ban roll-on antiperspirant deodorant satin breeze (source: ndc)
Generic Name aluminum chlorohydrate (source: ndc)
Application Number M019 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 g/103mL
source: ndc
Packaging
  • 4 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-339-14) / 103 mL in 1 BOTTLE, WITH APPLICATOR
  • 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-339-35)
  • 2 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-339-70) / 103 mL in 1 BOTTLE, WITH APPLICATOR
source: ndc

Packages (3)

10596-339-14 4 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-339-14) / 103 mL in 1 BOTTLE, WITH APPLICATOR 10596-339-35 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-339-35) 10596-339-70 2 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-339-70) / 103 mL in 1 BOTTLE, WITH APPLICATOR

Ingredients (1)

aluminum chlorohydrate (20 g/103mL)

Linked Drug Pages (1)

Ban Roll-On Antiperspirant Deodorant Satin Breeze ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "21d9bd72-4a57-8024-e063-6394a90a1df8", "openfda": {"upc": ["0019045010080"], "unii": ["HPN8MZW13M"], "spl_set_id": ["d6d6368f-489f-4d6b-bbc0-e2dfb7ec3f90"], "manufacturer_name": ["Kao USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-339-14)  / 103 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "10596-339-14", "marketing_start_date": "20200824"}, {"sample": false, "description": "103 mL in 1 BOTTLE, WITH APPLICATOR (10596-339-35)", "package_ndc": "10596-339-35", "marketing_start_date": "20120101"}, {"sample": false, "description": "2 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-339-70)  / 103 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "10596-339-70", "marketing_start_date": "20200824"}], "brand_name": "Ban Roll-On Antiperspirant Deodorant Satin Breeze", "product_id": "10596-339_21d9bd72-4a57-8024-e063-6394a90a1df8", "dosage_form": "LIQUID", "product_ndc": "10596-339", "generic_name": "Aluminum Chlorohydrate", "labeler_name": "Kao USA Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ban", "brand_name_suffix": "Roll-On Antiperspirant Deodorant Satin Breeze", "active_ingredients": [{"name": "ALUMINUM CHLOROHYDRATE", "strength": "20 g/103mL"}], "application_number": "M019", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120101", "listing_expiration_date": "20261231"}