notts - pain relief pm

Generic: acetaminophen, diphenhydramine hydrochloride

Labeler: vivunt pharma llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name notts - pain relief pm
Generic Name acetaminophen, diphenhydramine hydrochloride
Labeler vivunt pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, diphenhydramine hydrochloride 25 mg/1

Manufacturer
VIVUNT PHARMA LLC

Identifiers & Regulatory

Product NDC 82706-009
Product ID 82706-009_284f426f-6cb5-4e7e-e063-6294a90a946e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2022-08-17

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82706009
Hyphenated Format 82706-009

Supplemental Identifiers

RxCUI
1092189
UPC
0850047780041
UNII
362O9ITL9D TC2D6JAD40

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 notts - pain relief pm (source: ndc)
Generic Name acetaminophen, diphenhydramine hydrochloride (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (82706-009-01) / 24 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (82706-009-02) / 50 TABLET in 1 BOTTLE
source: ndc

Packages (2)

82706-009-01 1 BOTTLE in 1 CARTON (82706-009-01) / 24 TABLET in 1 BOTTLE 82706-009-02 1 BOTTLE in 1 CARTON (82706-009-02) / 50 TABLET in 1 BOTTLE

Ingredients (2)

acetaminophen (500 mg/1) diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

NOTTS - Pain Relief PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "284f426f-6cb5-4e7e-e063-6294a90a946e", "openfda": {"upc": ["0850047780041"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["e6754f62-e3b2-773f-e053-2a95a90ad36a"], "manufacturer_name": ["VIVUNT PHARMA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82706-009-01)  / 24 TABLET in 1 BOTTLE", "package_ndc": "82706-009-01", "marketing_start_date": "20220817"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (82706-009-02)  / 50 TABLET in 1 BOTTLE", "package_ndc": "82706-009-02", "marketing_start_date": "20220817"}], "brand_name": "NOTTS - Pain Relief PM", "product_id": "82706-009_284f426f-6cb5-4e7e-e063-6294a90a946e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "82706-009", "generic_name": "Acetaminophen, Diphenhydramine hydrochloride", "labeler_name": "VIVUNT PHARMA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NOTTS - Pain Relief PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220817", "listing_expiration_date": "20261231"}