United States· US:69729-070_2860afb9-3da9-5f80-e063-6394a90ab76b

Tenalif Children

A medicinal product containing acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide; guaifenesin, registered in United States by OPMX LLC.

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…normalisedTenalif ChildrenATC—REGISTER NO.US:69729-070_2860afb9…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Manufacturer
OPMX LLC
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
    6972907006
    1 BOTTLE, PLASTIC in 1 CARTON (69729-070-06) / 177 mL in 1 BOTTLE, PLASTIC
  • ndc11
    69729-070-06

Regulatory notes

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

Same medicine, other countries

Acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide; guaifenesin in 1 other country

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

All acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide; guaifenesin products

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/d7d26e88-9b38-480b-bea6-af157bbc5327
GET /v1/drugs/d7d26e88-9b38-480b-bea6-af157bbc5327?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": "250; 5; 13.33; 200",
  "substance": "ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
  "productndc": "69729-070",
  "dosage_form": "SYRUP",
  "dea_schedule": null,
  "strength_unit": "mg/10mL; mg/10mL; mg/10mL; mg/10mL",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide; guaifenesin.

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.