vicks zzzquil ultra

Generic: doxylamine succinate

Labeler: the procter & gamble manufacturing company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vicks zzzquil ultra
Generic Name doxylamine succinate
Labeler the procter & gamble manufacturing company
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxylamine succinate 25 mg/1

Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 69423-902
Product ID 69423-902_402e64c4-5771-d190-e063-6294a90a7fe2
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA040167
Listing Expiration 2026-12-31
Marketing Start 2021-03-01

Pharmacologic Class

Classes
antihistamine [epc] histamine receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69423902
Hyphenated Format 69423-902

Supplemental Identifiers

RxCUI
1101446 2548540
UPC
0323900042728
UNII
V9BI9B5YI2

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 vicks zzzquil ultra (source: ndc)
Generic Name doxylamine succinate (source: ndc)
Application Number ANDA040167 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1 TABLET in 1 POUCH (69423-902-01)
  • 1 BLISTER PACK in 1 CARTON (69423-902-12) / 12 TABLET in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (69423-902-24) / 12 TABLET in 1 BLISTER PACK
  • 32 POUCH in 1 CARTON (69423-902-32) / 1 TABLET in 1 POUCH
  • 4 BLISTER PACK in 1 CARTON (69423-902-48) / 12 TABLET in 1 BLISTER PACK
source: ndc

Packages (5)

Ingredients (1)

doxylamine succinate (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "402e64c4-5771-d190-e063-6294a90a7fe2", "openfda": {"upc": ["0323900042728"], "unii": ["V9BI9B5YI2"], "rxcui": ["1101446", "2548540"], "spl_set_id": ["c29f6f9a-7b55-30c3-e053-2995a90a9de7"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET in 1 POUCH (69423-902-01)", "package_ndc": "69423-902-01", "marketing_start_date": "20231016"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69423-902-12)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "69423-902-12", "marketing_start_date": "20210301"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (69423-902-24)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "69423-902-24", "marketing_start_date": "20210301"}, {"sample": false, "description": "32 POUCH in 1 CARTON (69423-902-32)  / 1 TABLET in 1 POUCH", "package_ndc": "69423-902-32", "marketing_start_date": "20231016"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (69423-902-48)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "69423-902-48", "marketing_start_date": "20210301"}], "brand_name": "Vicks ZzzQuil Ultra", "product_id": "69423-902_402e64c4-5771-d190-e063-6294a90a7fe2", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "69423-902", "generic_name": "Doxylamine succinate", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Vicks ZzzQuil", "brand_name_suffix": "Ultra", "active_ingredients": [{"name": "DOXYLAMINE SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA040167", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}