Package 11559-001-01

Brand: youth dew roll-on antiperspirant deodorant

Generic: aluminum chlorohydrate
NDC Package

Package Facts

Identity

Package NDC 11559-001-01
Digits Only 1155900101
Product NDC 11559-001
Product ID 11559-001_1d18cdb3-8500-c614-e063-6394a90aefca
Description

75 mL in 1 BOTTLE, WITH APPLICATOR (11559-001-01)

Marketing

Marketing Status
Marketed Since 2020-12-02
Brand youth dew roll-on antiperspirant deodorant
Generic aluminum chlorohydrate
Sample Package No

Linked Drug Pages (1)

YOUTH DEW ROLL-ON ANTIPERSPIRANT DEODORANT ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "1d18cdb3-8500-c614-e063-6394a90aefca", "openfda": {"upc": ["0027131007524"], "unii": ["HPN8MZW13M"], "spl_set_id": ["e2dd4147-673b-4c95-8171-fb9e841f2db6"], "manufacturer_name": ["ESTEE LAUDER INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE, WITH APPLICATOR (11559-001-01)", "package_ndc": "11559-001-01", "marketing_start_date": "20201202"}], "brand_name": "YOUTH DEW ROLL-ON ANTIPERSPIRANT DEODORANT", "product_id": "11559-001_1d18cdb3-8500-c614-e063-6394a90aefca", "dosage_form": "LIQUID", "product_ndc": "11559-001", "generic_name": "ALUMINUM CHLOROHYDRATE", "labeler_name": "ESTEE LAUDER INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "YOUTH DEW ROLL-ON ANTIPERSPIRANT DEODORANT", "active_ingredients": [{"name": "ALUMINUM CHLOROHYDRATE", "strength": "200 mg/mL"}], "application_number": "M019", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201202", "listing_expiration_date": "20261231"}