vicks childrens cough congestion night

Generic: phenylephrine hydrochloride and diphenhydramine hydrochloride

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

Drug Facts

Product Profile

Brand Name vicks childrens cough congestion night
Generic Name phenylephrine hydrochloride and diphenhydramine hydrochloride
Labeler the procter & gamble manufacturing company
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 12.5 mg/15mL, phenylephrine hydrochloride 5 mg/15mL

Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 37000-712
Product ID 37000-712_401e3b66-8fbf-8de9-e063-6394a90a4a1e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2019-04-22

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37000712
Hyphenated Format 37000-712

Supplemental Identifiers

RxCUI
2166129
UNII
TC2D6JAD40 04JA59TNSJ

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 childrens cough congestion night (source: ndc)
Generic Name phenylephrine hydrochloride and diphenhydramine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/15mL
  • 5 mg/15mL
source: ndc
Packaging
  • 177 mL in 1 BOTTLE, PLASTIC (37000-712-06)
source: ndc

Packages (1)

37000-712-06 177 mL in 1 BOTTLE, PLASTIC (37000-712-06)

Ingredients (2)

diphenhydramine hydrochloride (12.5 mg/15mL) phenylephrine hydrochloride (5 mg/15mL)

Linked Drug Pages (1)

Vicks childrens Cough Congestion Night ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "401e3b66-8fbf-8de9-e063-6394a90a4a1e", "openfda": {"unii": ["TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["2166129"], "spl_set_id": ["87231460-8b45-b995-e053-2a91aa0a6c43"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (37000-712-06)", "package_ndc": "37000-712-06", "marketing_start_date": "20190422"}], "brand_name": "Vicks childrens Cough Congestion Night", "product_id": "37000-712_401e3b66-8fbf-8de9-e063-6394a90a4a1e", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "37000-712", "generic_name": "Phenylephrine Hydrochloride and Diphenhydramine Hydrochloride", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Vicks childrens", "brand_name_suffix": "Cough Congestion Night", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/15mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/15mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190422", "listing_expiration_date": "20261231"}