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United States· US:66715-6615_450e8974-8ff9-4b82-e063-6394a90a9366

DayTime Relief, Cold and Flu, 24-7 Life by 7-Eleven

A medicinal product containing phenylephrine hydrochloride; dextromethorphan hydrobromide; acetaminophen, registered in United States by Lil' Drug Store Products, Inc..

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…normalisedDayTime Relief, Cold and Flu, 24-7 Li…ATC—REGISTER NO.US:66715-6615_450e897…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN
Manufacturer
Lil' Drug Store Products, Inc.
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 · 2

  • ndc11
    6671566154
    177 mL in 1 BOTTLE, PLASTIC (66715-6615-4)
  • ndc11
    66715-6615-4

Regulatory notes

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

Same medicine, other countries

Phenylephrine hydrochloride; dextromethorphan hydrobromide; acetaminophen in 2 other countries

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

All phenylephrine hydrochloride; dextromethorphan hydrobromide; acetaminophen products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Czechia · Paralen Grip Chřipka A Kašel
  • Slovakia · Paralen Grip Chrípka A Kašeľ

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/c0c3cbf2-f76c-47f1-bb94-c07fbb05aa19
GET /v1/drugs/c0c3cbf2-f76c-47f1-bb94-c07fbb05aa19?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": "5; 10; 325",
  "substance": "PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN",
  "productndc": "66715-6615",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "mg/15mL; mg/15mL; mg/15mL",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about phenylephrine hydrochloride; dextromethorphan hydrobromide; acetaminophen.

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.