Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Eyes Alive Lubricating CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 5 mg/mL Liquid, 100 ampules — NDC 83291-200-00 (Billing 83291-0200-00)
by RIVIERA PHARMA INC · 100 AMPULE in 1 CARTON / .6 mL in 1 AMPULE
This is a package of 100 ampules of Eyes Alive Lubricating CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 5 mg/mL Liquid from RIVIERA PHARMA INC, marketed since Jun 2023 and currently FDA-listed. It is the main listing for this product, which comes in 7 package sizes.
NDC 83291-0200-00
🏷️ FDA NDC (as labeled)
83291-200-00
billing pads the product segment with a zero
This package
Contains100 ampules
Pack sizes7 compare ↓
Main listing for product 83291-200 · Also comes in:
2 ampules 83291-200-02
4 ampules 83291-200-04
8 ampules 83291-200-08
32 ampules 83291-200-32
52 ampules 83291-200-52
72 ampules 83291-200-72
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
83291-200-00
Product NDC
83291-200
11-digit billing NDC
83291020000
UNII
K679OBS311
UPC
0383291000035
Application #
M018
SPL Set ID
b6966691-6884-438c-9f89-5924089226e1
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2023-06-01
Route
INTRAOCULAR
Dosage form
LIQUID
Substance
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification
GPI-14
86200010102021
GCN Seq No
030011
GCN
37384
HICL code
003843
Ingredient (HICL)
Carboxymethylcellulose Sodium
HIC1 code
Q
Therapeutic class — broad (HIC1)
Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code
Q6
Therapeutic class — intermediate (HIC2)
Ophthalmic Preparations
HIC3 code
Q6T
Therapeutic class — specific (HIC3)
Artificial Tears
AHFS code
52:92.00.00
AHFS class
Eent Drugs, Miscellaneous
FDB label name
EYES ALIVE LUB 0.5% EYE DROPS
FDB brand name
Eyes Alive
Legend status
O — Over-the-counter (OTC) drug or device
Quick answers
- GSN (GCN sequence number): 030011
- GCN: 37384
- GPI-14 (Medi-Span): 86200010102021
- HICL (First Databank): 003843
- AHFS class code: 52:92.00.00
- RxCUI (RxNorm): 1188426
Why two NDCs?
The FDA registers this code as 83291-200-00 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 83291-0200-00. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
Label name EYES ALIVE LUB 0.5% EYE DROPS Ingredient Carboxymethylcellulose Sodium
🧪 What is this product?
Eyes Alive Lubricating is an over-the-counter eye drop solution containing carboxymethylcellulose sodium, a lubricating ingredient typically used to relieve dry eye discomfort and irritation. The product is applied directly to the eye surface to help coat and moisturize the ocular tissues. Carboxymethylcellulose sodium functions as an artificial tear substitute, commonly used to temporarily soothe dryness and provide a protective layer on the eye.
Patient education
Supplement & herbal interactions
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per mL | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 3, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 83291-0200-00 You're viewing this Main listing | 100 AMPULE in 1 CARTON / .6 mL in 1 AMPULE | 2023-06-01 | — | Active |
| 83291-0200-02 83291-200-02 | 2 AMPULE in 1 POUCH / .6 mL in 1 AMPULE | 2023-06-01 | — | Active |
| 83291-0200-04 83291-200-04 | 4 AMPULE in 1 POUCH / .6 mL in 1 AMPULE | 2023-06-01 | — | Active |
| 83291-0200-08 83291-200-08 | 8 AMPULE in 1 CARTON / .6 mL in 1 AMPULE | 2023-06-01 | — | Active |
| 83291-0200-32 83291-200-32 | 32 AMPULE in 1 CARTON / .6 mL in 1 AMPULE | 2023-06-01 | — | Active |
| 83291-0200-52 83291-200-52 | 52 AMPULE in 1 CARTON / .6 mL in 1 AMPULE | 2023-06-01 | — | Active |
| 83291-0200-72 83291-200-72 | 72 AMPULE in 1 CARTON / .6 mL in 1 AMPULE | 2023-06-01 | — | Active |
Pack size FAQ
What quantity is in this package?
This package contains 100 ampules — 100 ampule in 1 carton / .6 ml in 1 ampule.
How does this package differ from NDC 83291-0200-02?
Both are Eyes Alive Lubricating CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 5 mg/mL Liquid — the drug itself is identical. This page's package is the 100 ampules one, while NDC 83291-0200-02 is the 2 ampules package.
What NDC number is used to bill for this package of Eyes Alive Lubricating CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 5 mg/mL Liquid?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Leader Lubricant Eye Drops .5 g/100mL 70000-0012-01 | Cardinal | 70 vials | $0.163 | — | Availability likely | — |
| Rugby Lubricant Eye Drops .5 g/100mL 00536-1387-92 | Rugby | 30 vials | $0.227 | — | Availability likely | — |
| Good Neighbor Pharmacy Lubricant Eye Drops .5 g/100mL 46122-0756-56 | Amerisource | 30 vials | $0.227 | — | Availability likely | — |
| carboxymethylcellulose sodium 5 mg/mL 50268-0067-30 | AvPAK | 30 vials | $0.227 | — | Availability likely | — |
| Foster and Thrive Lubricant Eye Drops .5 g/100mL 70677-1190-01 | Strategic | 30 vials | $0.227 | — | Availability likely | — |
| Carboxymethylcellulose Sodium Eye Lubricant 5 mg/mL 42494-0448-05 | Cameron | 2 bottles | $0.275 | — | Discontinued | — |
| Rugby Carboxymethylcellulose Sodium 0.5% Eye Drops .5 g/100mL 00536-1386-35 | Rugby | 2 bottles | $0.280 | — | Availability likely | — |
| carboxymethylcellulose sodium 5 mg/mL 50268-0068-15 | AvPAK | 1 bottle | $0.324 | — | Availability likely | — |
| Leader Lubricant Eye Drops Soothing Relief .5 g/100mL 70000-0705-01 | LEADER/Cardinal | 1 bottle | $0.324 | — | Availability likely | — |
| Refresh Tears 5 mg/mL 00023-0798-01 | Allergan, | 2 bottles | $0.412 | — | Availability likely | — |
| Lubricant Drops 5 mg/mL 70000-0090-01 | CARDINAL | 1 bottle | $0.498 | — | FDA listed | — |
| Refresh Plus 5 mg/mL 00023-0403-05 | Allergan, | 5 vials | — | — | FDA listed | — |
| Refresh Tears 00023-0795-65 | Allergan, | 1 kit | — | — | FDA listed | — |
| Walgreens Lubricant Eye Drops Preservative Free .5 g/100mL 00363-8800-01 | Walgreen | 30 vials | — | — | FDA listed | — |
| Walgreens Lubricant Eye Drops 5 mg/mL 00363-8832-15 | Walgreen | 2 bottles | — | — | FDA listed | — |
| Walgreens Lubricant Eye Drops 5 mg/mL 00363-8833-15 | Walgreen | 1 bottle | — | — | FDA listed | — |
| Lubricant Eye 5 mg/mL 00536-1476-92 | Rugby | 30 ampules | — | — | FDA listed | — |
| Lubricant Eye Drops Preservative Free .5 g/100mL 11673-0150-01 | Target | 70 vials | — | — | FDA listed | — |
| Up and Up Dry Eye Relief Lubricant Eye Drops 5 mg/mL 11673-0771-01 | Target | 2 bottles | — | — | FDA listed | — |
| Up and Up Dry Eye Relief Lubricant Eye Drops 5 mg/mL 11716-0771-01 | Hanlim | 2 bottles | — | — | FDA listed | — |
| Auro-Cmc 5 mg/mL 16030-0401-10 | Aurolab | 10 ml | — | — | FDA listed | — |
| Carboxymethylcellulose Sodium Eye Drops 0.5% 5 mg/mL 16030-0501-05 | Aurolab | 5 ml | — | — | FDA listed | — |
| Gentle Eyes Lubricant Eye Drops 5 mg/mL 17312-0430-15 | TRP | 1 bottle | — | — | FDA listed | — |
| Signature Care Lubricant Eye Drops .5 g/100mL 21130-0705-01 | Better | 30 vials | — | — | FDA listed | — |
| Kroger Lubricant Eye .5 g/100mL 30142-0373-33 | The | 30 vials | — | — | FDA listed | — |
| HEB Lubricant Eye Drops .5 g/100mL 37808-0100-01 | HEB | 30 vials | — | — | FDA listed | — |
| Medi-First Lubricant Eye Drops .5 g/100mL 47682-0193-83 | Unifirst | 30 ampules | — | — | FDA listed | — |
| Green Guard Lubricant Eye Drops .5 g/100mL 47682-0194-83 | UniFirst | 30 ampules | — | — | FDA listed | — |
| Equate Lubricant Eye Drops Preservative-Free .5 g/100mL 49035-0245-01 | Wal-Mart | 25 vials | — | — | FDA listed | — |
| Equate Restore Plus Lubricant Eye Drops .5 g/100mL 49035-0389-01 | Walmart, | 70 vials | — | — | FDA listed | — |
| Good Sense Lubricating Plus Lubricant Eye Drops .5 g/100mL 50804-0700-01 | GoodSense | 30 bottles | — | — | FDA listed | — |
| Carboxymethylcellulose Sodium 0.5% 5 mg/mL 51407-0945-30 | Golden | 3 pouches | — | — | Discontinued | — |
| Discount Drug Mart Lubricant Eye Drops 5 mg/mL 53943-0510-01 | Discount | 5 bottles | — | — | FDA listed | — |
| Retaine CMC 5 mg/mL 54799-0460-30 | OCuSOFT | 30 vials | — | — | FDA listed | — |
| Medics Choice Lubricant Eye Drops .5 g/100mL 55651-0030-01 | K.C. | 5 ampules | — | — | FDA listed | — |
| Lubricant Eye Drops 5 mg/mL 55651-0105-05 | KC | 5 bottles | — | — | FDA listed | — |
| Lubricant Eye Drops 5 mg/mL 55651-0510-01 | KC | 5 bottles | — | — | FDA listed | — |
| Publix Moisturizing Relief Eye Drops .5 g/100mL 56062-0789-01 | Publix | 30 vials | — | — | FDA listed | — |
| TheraTears Dry and Tired 5 mg/mL 58790-0013-30 | MEDTECH | 6 pouches | — | — | FDA listed | — |
| Family Care Single Use Lubricant Eye Drop 0.4mL 5ct 5 mg/mL 65923-0575-05 | United | 1 vial | — | — | FDA listed | — |
| Family Care Single Use Lubricant Eye Drop 0.4mL 30ct 5 mg/mL 65923-0576-30 | United | 30 vials | — | — | FDA listed | — |
| Refresh Tears 5 mg/mL 66715-1073-00 | Lil' | 1 bottle | — | — | Discontinued | — |
| Refresh Tears Lubricant 5 mg/mL 67751-0130-01 | Navajo | 3 ml | — | — | Discontinued | — |
| Lubricating Tears 5 mg/mL 69618-0076-55 | Reliable | 1 bottle | — | — | FDA listed | — |
| CVS Lubricant Eye Drops .5 g/100mL 69842-0804-01 | CVS | 70 vials | — | — | FDA listed | — |
| CVS Lubricant Eye Drops 30 ct .5 g/100mL 69842-0993-01 | CVS | 30 vials | — | — | FDA listed | — |
| Lubricant Eye 5 mg/mL 70000-0751-01 | CARDINAL | 30 ampules | — | — | FDA listed | — |
| Lubricant Eye Drops 5 mg/mL 71105-0105-05 | Redicare | 5 bottles | — | — | FDA listed | — |
| TopCare Health Lubricant Eye Drops .5 g/100mL 76162-0089-30 | Topcare | 30 vials | — | — | FDA listed | — |
| Meijer Lubricant Eye Drops .5 g/100mL 79481-0066-01 | Meijer | 30 vials | — | — | FDA listed | — |
| Rain Renewal Eye Drops .5 g/100mL 79662-0001-30 | Rain | 30 bottles | — | — | FDA listed | — |
| Equate Moisturizing Comfort Lubricant Eye Drops .5 g/100mL 79903-0264-05 | Walmart | 1 bottle | — | — | FDA listed | — |
| Focus Tears PF 5 mg/mL 82724-0009-20 | Covalent | 30 vials | — | — | FDA listed | — |
| Eyes Alive Lubricating 5 mg/mLthis 83291-0200-00 | RIVIERA | 100 ampules | — | — | FDA listed | — |
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2023
On the market since
Jun 2023
📍
2026
Currently FDA-listed
3 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
- FDA Orange Book · refreshed Sep 3, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII M4I0D6VV5M
Calcium chloride is a salt compound that acts as a firming agent and source of calcium ions in medications. It's used in formulations to help maintain tablet structure, improve texture, or serve as a buffering agent.
-
UNII QTT17582CB
A strong acid used to adjust and maintain the proper pH level in liquid medicines, ensuring stability and preventing breakdown of active ingredients.
-
UNII 02F3473H9O
A mineral salt used in medications as a source of magnesium. It helps bind ingredients together, improve texture, and maintain the product's stability during storage.
-
UNII 660YQ98I10
Potassium chloride is a mineral salt used in medicines as a buffer and to help maintain the proper pH balance and stability of the formulation during storage and use.
-
UNII 451W47IQ8X
Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
-
UNII 55X04QC32I
A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
-
UNII TU7HW0W0QT
A salt derived from lactic acid, sodium lactate acts as a buffer and pH stabilizer in medicines. It helps maintain the product's acidity level and can also serve as a humectant to retain moisture.
-
UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
8 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesCalcium chloride, hydrochloric acid May or may not contain this ingredient to adjust pH., magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide, and sodium lactate.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed —
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
Manufacturer & labeler
LabelerRIVIERA PHARMA INC
FDA applicationM018 (OTC MONOGRAPH DRUG)
Labeler code83291
First marketedJun 2023
Product typeHuman Otc Drug
Portfolio2 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Do Not Use
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun. may be used as a protectant against further irritation of the eye.
⏱️ Dosage and Administration ▾
Directions TWIST AND REMOVE TAB Place 1 or 2 drops in the affected eye(s) as needed for relief and discard container. If used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctors instructions.
⚠️ Warnings ▾
Warnings For external use only Do not use is solution changes color or becomes cloudy. When using this product to avoid contamination, do not touch tip of container to any surface. Do not reuse.
Once open, discard. do not touch unit dose tip to eye Stop use and ask a doctor before use if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours. Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center right away.
📦 Storage and Handling ▾
Other information Use only if single use container is intact. Use before expiration date marked on container. Store at 59°-86°F (15°-30°C) RETAIN THIS CARTON FOR FUTURE REFERENCE.
🧪 Active Ingredient ▾
Active ingredients Carboxymethylcellulose sodium 0.5%
🧪 Inactive Ingredients ▾
Inactive ingredients Calcium chloride, hydrochloric acid May or may not contain this ingredient to adjust pH. , magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide , and sodium lactate.
🎯 Purpose ▾
Purpose Eye lubricant
📄 Do Not Use ▾
Do not use is solution changes color or becomes cloudy.
📄 When Using This Product ▾
When using this product to avoid contamination, do not touch tip of container to any surface. Do not reuse. Once open, discard. do not touch unit dose tip to eye
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor before use if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center right away.
📄 Questions or Comments ▾
Questions or comments? 800.477.2884, M-F 8AM-5PM Eastern Time You can always report serious effects to this number.
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL - 0.6 mL Container Carton NDC 83291-200-32 Eyes Alive ™ Lubricating Eye Drops Carboxymethylcellulose sodium 0.5% Preservative Free IMMEDIATE RELIEF FOR DRY IRRITATED EYES 32 Sterile Single-Use Containers 0.02 fl oz (0.6 mL) each MADE IN THE USA Principal Display Panel - 0.6 mL Container Carton
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
About this NDC listing & data coverage
Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by RIVIERA PHARMA INC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 6 other package presentations of this same product, including 2 ampules (83291-0200-02), 4 ampules (83291-0200-04), 8 ampules (83291-0200-08). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
RIVIERA PHARMA INC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.