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United States· US:58790-000_39e5aaf6-e4a0-4167-b458-f22af5906ddc

TheraTears Lubricant

A medicinal product containing carboxymethylcellulose sodium, unspecified form, registered in United States by MEDTECH 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…normalisedTheraTears LubricantATC—REGISTER NO.US:58790-000_39e5aaf6…PACKS LISTED10CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
Manufacturer
MEDTECH 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 · 10

  • ndc11
    5879000000
    6 POUCH in 1 CARTON (58790-000-00) / 5 VIAL in 1 POUCH / .6 mL in 1 VIAL
  • ndc11
    5879000020
    5 POUCH in 1 CARTON (58790-000-20) / 4 APPLICATOR in 1 POUCH / 19.2 mL in 1 APPLICATOR
  • ndc11
    5879000024
    6 POUCH in 1 CARTON (58790-000-24) / 4 APPLICATOR in 1 POUCH / 19.2 mL in 1 APPLICATOR
  • ndc11
    5879000030
    6 POUCH in 1 CARTON (58790-000-30) / 5 VIAL in 1 POUCH / .6 mL in 1 VIAL
  • ndc11
    5879000032
    8 POUCH in 1 CARTON (58790-000-32) / 4 APPLICATOR in 1 POUCH / 19.2 mL in 1 APPLICATOR
  • ndc11
    58790-000-00
  • ndc11
    58790-000-20
  • ndc11
    58790-000-24
  • ndc11
    58790-000-30
  • ndc11
    58790-000-32

Regulatory notes

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

Same medicine, other countries

Carboxymethylcellulose sodium, unspecified form in 2 other countries

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

All carboxymethylcellulose sodium, unspecified form 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/d8ca7d25-6485-4026-8a84-8ff757ce3940
GET /v1/drugs/d8ca7d25-6485-4026-8a84-8ff757ce3940?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": "OPHTHALMIC",
  "source": "ndc",
  "strength": "2.5",
  "substance": "CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM",
  "productndc": "58790-000",
  "dosage_form": "SOLUTION/ DROPS",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about carboxymethylcellulose sodium, unspecified form.

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.