United States· US:83291-200_7b0dddfc-9933-4f2f-840f-7a7b28cbf1fa

Eyes Alive

A medicinal product containing carboxymethylcellulose sodium, unspecified, registered in United States by RIVIERA PHARMA 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…normalisedEyes AliveATC—REGISTER NO.US:83291-200_7b0dddfc…PACKS LISTED14CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Manufacturer
RIVIERA PHARMA 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 · 14

  • ndc11
    83291-200-00
  • ndc11
    83291-200-02
  • ndc11
    83291-200-04
  • ndc11
    83291-200-08
  • ndc11
    83291-200-32
  • ndc11
    83291-200-52
  • ndc11
    83291-200-72
  • ndc11
    8329120000
    100 AMPULE in 1 CARTON (83291-200-00) / .6 mL in 1 AMPULE
  • ndc11
    8329120002
    2 AMPULE in 1 POUCH (83291-200-02) / .6 mL in 1 AMPULE
  • ndc11
    8329120004
    4 AMPULE in 1 POUCH (83291-200-04) / .6 mL in 1 AMPULE
  • ndc11
    8329120008
    8 AMPULE in 1 CARTON (83291-200-08) / .6 mL in 1 AMPULE
  • ndc11
    8329120032
    32 AMPULE in 1 CARTON (83291-200-32) / .6 mL in 1 AMPULE
  • ndc11
    8329120052
    52 AMPULE in 1 CARTON (83291-200-52) / .6 mL in 1 AMPULE
  • ndc11
    8329120072
    72 AMPULE in 1 CARTON (83291-200-72) / .6 mL in 1 AMPULE

Regulatory notes

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

Same medicine, other countries

Carboxymethylcellulose sodium, unspecified 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 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/a21ee975-1a88-4c38-ab8d-882e8e1e265f
GET /v1/drugs/a21ee975-1a88-4c38-ab8d-882e8e1e265f?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": "INTRAOCULAR",
  "source": "ndc",
  "strength": "5",
  "substance": "CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED",
  "productndc": "83291-200",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about carboxymethylcellulose sodium, unspecified.

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.