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United States· US:30142-755_0ff0d79b-98ed-4c9f-b57c-2553cb9cb784

Extra Strength Acetaminophen PM

A medicinal product containing acetaminophen; diphenhydramine hydrochloride, registered in United States by KROGER COMPANY.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedExtra Strength Acetaminophen PMATC—REGISTER NO.US:30142-755_0ff0d79b…PACKS LISTED6CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Manufacturer
KROGER COMPANY
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 6

  • ndc11
    30142-755-01
  • ndc11
    30142-755-05
  • ndc11
    30142-755-20
  • ndc11
    3014275501
    1 BOTTLE in 1 CARTON (30142-755-01) / 100 TABLET in 1 BOTTLE
  • ndc11
    3014275505
    1 BOTTLE in 1 CARTON (30142-755-05) / 50 TABLET in 1 BOTTLE
  • ndc11
    3014275520
    2 BOTTLE in 1 CARTON (30142-755-20) / 100 TABLET in 1 BOTTLE

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Acetaminophen; diphenhydramine hydrochloride in 6 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All acetaminophen; diphenhydramine hydrochloride products

Authorised across Europe · EMA

The same active substance is authorised in 6 EEA countries. Names it is sold under:

  • Spain · Dolomidina
  • United Kingdom (Northern Ireland) · Panadol Night, Panadol Nightpain
  • Ireland · Dozol, Panadol Night
  • Malta · Dozol, Teedex
  • Poland · Apap Noc, Paracetamol + Difenhydramina Noc Hasco
  • Portugal · Algik Noite, Chrobion

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/cfac37c2-339e-40bd-9cbe-1c2d6975049e
GET /v1/drugs/cfac37c2-339e-40bd-9cbe-1c2d6975049e?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "500; 25",
  "substance": "ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE",
  "productndc": "30142-755",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1",
  "application_number": "M013",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about acetaminophen; diphenhydramine hydrochloride.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.