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by selected hyaluron day serum Niacinamide 1 g/50mL Liquid, 50 mL

by Garam Of Nature · 1 CONTAINER in 1 CARTON (73509-030-02) / 50 mL in 1 CONTAINER (73509-030-01)
NDC 73509-0030-02
🏷️ FDA NDC (as labeled) 73509-030-02 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Inactivated by FDA
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 73509-030-02
Product NDC 73509-030
11-digit billing NDC 73509003002
UNII 25X51I8RD4
UPC 8809154465084
SPL Set ID 64d32e46-8bb9-45d2-995d-faa546cbfbda
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2019-12-01
Route TOPICAL
Dosage form LIQUID
Substance NIACINAMIDE
Why two NDCs? The FDA registers this code as 73509-030-02 — 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 → 73509-0030-02. 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.

🏭 Manufacturer & labeler

LabelerGaram Of Nature
Labeler code73509
First marketedDec 2019
Product typeHuman Otc Drug
Portfolio6 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.

🩺 Clinical

🧪 What is this product?

This is a topical liquid serum containing niacinamide (vitamin B3) at a concentration of 1 g per 50 mL. Niacinamide is commonly used in skincare products for its role in supporting skin barrier function and reducing irritation. This product is an unapproved drug and has not received FDA marketing approval.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

🧪 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 PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • 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.

2 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive ingredients: Water, Glycerin, Butylene Glycol, 1,2-Hexanediol, Polyglyceryl-10 Oleate, Silk Amino Acids, Angelica Dahurica Root Extract, Cimicifuga Dahurica Root Extract, Bletia Hyacinthina Bulb Extract, Oryza Sativa (Rice) Extract, Phaseolus Radiatus Seed Extract, Trichosanthes Kirilowii Root Extract, Amomum Xanthioides Seed Extract, Broussonetia Kazinoki Root Extract, Eugenia Caryophyllus (Clove) Flower Extract, Sodium Hyaluronate, Allantoin, Rehmannia Chinensis Root Extract, Poria Cocos Extract, Panax Ginseng Root Extract, Honey Extract, Pentylene Glycol, Glyceryl Acrylate/Acrylic Acid Copolymer, Ethylhexylglycerin, Phenoxyethanol, Hydrogenated Lecithin, Caprylyl glycol, Camellia Japonica Seed Oil, Disodium EDTA, Sucrose Palmitate, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Hydrogenated Lecithin, Aniba Rosodora (Rosewood) Wood Oil, Santalum Album (Sandalwood) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Citrus Limon (Lemon) Peel Oil, Olea Europaea (Olive) Fruit Oil, Macadamia Integrifolia Seed Oil, Vitis Vinifera (Grape) Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Hyaluronate Crosspolymer, Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Palmitoyl Hexapeptide-12, Hydrolyzed Hyaluronic Acid

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.

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.

💲 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 systemPer mLPer 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
by selected hyaluron day serum 1 g/50mLthis 73509-0030-02 Garam 50 ml — — Discontinued —
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.

⏳ Availability & generic status

🏛️
2019
On the market since
Dec 2019
📍
2026
Currently FDA-listed
7 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
73509-0030-02 You're viewing this 1 CONTAINER in 1 CARTON (73509-030-02) / 50 mL in 1 CONTAINER (73509-030-01) 2019-12-01 Inactivated by FDA

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Marketed without an FDA application No longer marketed (per FDA listing data)

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

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 — Not published for this NDC No photo available yet for this listing.
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 "Unapproved Drug Other". 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 FDA registers it as 73509-030-02, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 73509-0030-02, written without dashes as 73509003002. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 73509-0030-02, the first segment (73509) is the labeler code FDA assigned to Garam Of Nature; the middle segment (0030) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.
Who lists this product with the FDA?
Garam Of Nature 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.

📄 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 5 words ▾

Uses Uses: Helps skin whitening.

⏱️ Dosage and Administration 11 words ▾

Directions Directions: Apply the proper amount to your skin and evenly

⚠️ Warnings 146 words ▾

WARNINGS Warnings: 1. In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage 2) In case of having the same symptoms above on the part you put this product on by direct sunlight 2.

You are banned to use it on the part where you have a scar, eczema, or dermatitis 3. In case of getting it into your eyes, you have to wash it immediately 4. Caution for treatment and keeping 1) Tighten the lid after using it 2) Keep it out of infants or children's reach 3) Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight

🧪 Active Ingredient 6 words ▾

ACTIVE INGREDIENT Active ingredients: Niacinamide 2.0%

🧪 Inactive Ingredients 147 words ▾

INACTIVE INGREDIENT Inactive ingredients: Water, Glycerin, Butylene Glycol, 1,2-Hexanediol, Polyglyceryl-10 Oleate, Silk Amino Acids, Angelica Dahurica Root Extract, Cimicifuga Dahurica Root Extract, Bletia Hyacinthina Bulb Extract, Oryza Sativa (Rice) Extract, Phaseolus Radiatus Seed Extract, Trichosanthes Kirilowii Root Extract, Amomum Xanthioides Seed Extract, Broussonetia Kazinoki Root Extract, Eugenia Caryophyllus (Clove) Flower Extract, Sodium Hyaluronate, Allantoin, Rehmannia Chinensis Root Extract, Poria Cocos Extract, Panax Ginseng Root Extract, Honey Extract, Pentylene Glycol, Glyceryl Acrylate/Acrylic Acid Copolymer, Ethylhexylglycerin, Phenoxyethanol, Hydrogenated Lecithin, Caprylyl glycol, Camellia Japonica Seed Oil, Disodium EDTA, Sucrose Palmitate, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Hydrogenated Lecithin, Aniba Rosodora (Rosewood) Wood Oil, Santalum Album (Sandalwood) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Citrus Limon (Lemon) Peel Oil, Olea Europaea (Olive) Fruit Oil, Macadamia Integrifolia Seed Oil, Vitis Vinifera (Grape) Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Hyaluronate Crosspolymer, Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Palmitoyl Hexapeptide-12, Hydrolyzed Hyaluronic Acid

🎯 Purpose 4 words ▾

PURPOSE Purpose: Skin Brightening

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 73509-0020-02 · Garam 73509-0040-02 · Garam →
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.