United States· US:0023-0403_8fc924b2-2bb1-46ac-845b-41ef1570380e

REFRESH PLUS

A medicinal product containing carboxymethylcellulose sodium, registered in United States by Allergan, 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…normalisedREFRESH PLUSATC—REGISTER NO.US:0023-0403_8fc924b2…PACKS LISTED10CHECKEDAugust 2, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer
Allergan, Inc.
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
August 2, 2026

Packs & prices · 10

  • ndc11
    0023040305
    5 VIAL, SINGLE-USE in 1 CARTON (0023-0403-05) / .4 mL in 1 VIAL, SINGLE-USE
  • ndc11
    0023040310
    100 VIAL, SINGLE-USE in 1 CARTON (0023-0403-10) / .4 mL in 1 VIAL, SINGLE-USE
  • ndc11
    0023040330
    30 VIAL, SINGLE-USE in 1 CARTON (0023-0403-30) / .4 mL in 1 VIAL, SINGLE-USE
  • ndc11
    0023040350
    50 VIAL, SINGLE-USE in 1 CARTON (0023-0403-50) / .4 mL in 1 VIAL, SINGLE-USE
  • ndc11
    0023040370
    70 VIAL, SINGLE-USE in 1 CARTON (0023-0403-70) / .4 mL in 1 VIAL, SINGLE-USE
  • ndc11
    0023-0403-05
  • ndc11
    0023-0403-10
  • ndc11
    0023-0403-30
  • ndc11
    0023-0403-50
  • ndc11
    0023-0403-70

Regulatory notes

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

Same medicine, other countries

Carboxymethylcellulose sodium 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 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/025af1de-2bfd-43f6-9537-6abab980d93d
GET /v1/drugs/025af1de-2bfd-43f6-9537-6abab980d93d?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": "5",
  "substance": "CARBOXYMETHYLCELLULOSE SODIUM",
  "productndc": "0023-0403",
  "dosage_form": "SOLUTION/ DROPS",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about carboxymethylcellulose sodium.

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.