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ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB Zinc Oxide Octocrylene Ethylhexyl Salicylate Homosalate Titanium Dioxide 8 g/100mL; 10 g/100mL; 3 g/100mL; 8 g/100mL; 4 g/100mL Lotion, 60 mL — NDC 87719-0002-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB Zinc Oxide Octocrylene Ethylhexyl Salicylate Homosalate Titanium Dioxide 8 g/100mL; 10 g/100mL; 3 g/100mL; 8 g/100mL; 4 g/100mL Lotion, 60 mL — NDC 87719-002-01 (Billing 87719-0002-01)

by HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED · 60 mL in 1 BOTTLE

This is a package of 60 mL of ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB Zinc Oxide Octocrylene Ethylhexyl Salicylate Homosalate Titanium Dioxide 8 g/100mL; 10 g/100mL; 3 g/100mL; 8 g/100mL; 4 g/100mL Lotion from HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED, marketed since Jun 2026 and currently FDA-listed. It is this product's only package size.

NDC 87719-0002-01
🏷️ FDA NDC (as labeled) 87719-002-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87719-002-01
Product NDC 87719-002
11-digit billing NDC 87719000201
UNII V06SV4M95S, SOI2LOH54Z, 15FIX9V2JP, 5A68WGF6WM, 4X49Y0596W
UPC 0729238218338
Application # M020
SPL Set ID 5354af18-50c4-5fba-e063-6394a90ace39
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-06-03
Route TOPICAL
Dosage form LOTION
Substance HOMOSALATE; ZINC OXIDE; TITANIUM DIOXIDE; OCTOCRYLENE; ETHYLHEXYL SALICYLATE
Why two NDCs? The FDA registers this code as 87719-002-01 — 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 → 87719-0002-01. 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.

Clinical

🧪 What is this product?

Anessa Perfect UV Sunscreen Skincare Milk is a topical lotion marketed as an over-the-counter sunscreen product under FDA monograph rules. It contains five active ingredients that function as ultraviolet (UV) filters: ethylhexyl salicylate, homosalate, and octocrylene are chemical UV absorbers, while zinc oxide and titanium dioxide are mineral UV reflectants. These ingredients are typically combined in sunscreen formulations to help protect skin from sun exposure. The product is applied to skin as a lotion.

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.

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 gPer 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
87719-0002-01 You're viewing this Main listing 60 mL in 1 BOTTLE 2026-06-03 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Anessa Perfect Uv Sunscreen Skincare Milk Gb 8 g/100mL; 10 g/100mL; 3 g/100mL; 8 g/100mL; 4 g/100mLthis 87719-0002-01 HONGKONG 60 ml — — 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.

Availability & generic status

🏛️
2026
On the market since
Jun 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 5QB0T2IUN0
    Aluminum hydroxide is a white powder mineral compound used as an antacid ingredient in some formulations. It works as a buffer and pH regulator to help neutralize stomach acid in the medicine.
  • UNII 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • UNII PWZ1720CBH
    A chemical compound used as an ultraviolet light filter in topical formulations. It helps protect the medicine or product from degradation caused by sun exposure during storage and use.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII JU3D414057
    A natural plant extract from tangerine fruit peel used as a flavoring agent and color contributor. It adds tangerine taste and may provide a slight orange tint to medicines.
  • UNII 89B2BSF9I3
    A synthetic compound made by chemically combining corn dextrin (a starch derivative) with palmitic acid. It acts as a binder and flow agent, helping hold tablet ingredients together and improve powder handling during manufacturing.
  • UNII ANQ870JD20
    A synthetic chemical compound used as a UV filter in topical formulations. It protects the medicine or product from degradation caused by sunlight exposure during storage and use.
  • UNII J8T3X564IH
    A clear oily liquid derived from sebacic acid, used as a plasticizer and solvent in pharmaceutical coatings and films to improve flexibility and help active ingredients dissolve properly.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII CA2Y0FE3FX
    A salt derived from licorice root extract, used as a flavoring agent and sweetener. It may also help soothe and protect mucous membranes in throat lozenges and cough products.
  • UNII X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII 420IP921MB
    A chelating agent derived from edetic acid that binds to metals in the formulation. It helps stabilize the medicine by preventing metal ions from causing breakdown or discoloration.
  • UNII XQN8R9SAK4
    A synthetic ultraviolet filter compound used in topical formulations to absorb and protect against harmful UV rays. It functions as an active sunscreen agent rather than a traditional inactive filler or binder.
  • 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 918X1OUF1E
    Isohexadecane is a synthetic hydrocarbon oil used as an emollient and solvent in topical medicines. It helps dissolve active ingredients and improves spreadability and absorption through the skin.
  • UNII 0RE8K4LNJS
    Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
  • UNII X33R8U0062
    Isostearic acid is a fatty acid derived from vegetable oils. It acts as an emulsifier and lubricant in medicines, helping blend ingredients together and reducing friction during tablet or capsule manufacturing.
  • UNII Y4P927Q133
    Lauryl betaine is a gentle cleansing agent derived from coconut oil. It helps dissolve and mix other ingredients in liquid formulations and can reduce foam or improve texture in topical products.
  • UNII YK3DC63Y5M
    A mineral compound derived from natural or synthetic sources that acts as an anti-caking agent and flow aid. It helps prevent clumping and improves the powder's ability to flow smoothly during manufacturing and tablet formation.
  • UNII 8JC99XGU4W
    Soluble fish skin collagen is a protein derived from fish skin that acts as a binder and thickening agent in medicines. It helps hold ingredients together and gives the product the right texture or consistency.
  • UNII CUQ3A77YXI
    Panax ginseng root is a plant extract traditionally used in herbal preparations. In medications, it may serve as an active botanical ingredient or be included for flavoring and as a natural preservative or binder in formulations.
  • UNII A2Q2LHC6MA
    A synthetic fragrance compound used to add pleasant scent to medications. It serves as a flavoring and masking agent to make the medicine more palatable and appealing to patients.
  • UNII 8PR7V1SVM0
    A silicone-based lubricant combined with polyethylene glycol. It reduces friction and helps the medicine flow smoothly during manufacturing and improves how the product feels when applied or swallowed.
  • UNII 5655G9Y8AQ
    A synthetic liquid polymer used as a solvent and humectant in medications. It helps dissolve active ingredients, maintain moisture in the formulation, and improve how the medicine flows and is absorbed.
  • UNII TYP81E471F
    A silicone-based lubricant and anti-foaming agent derived from dimethicone, a synthetic polymer. It helps reduce friction during tablet or capsule manufacturing and prevents excessive foam in liquid formulations.
  • UNII 6DNW9T7YT2
    A synthetic liquid polymer made from ethylene and propylene compounds. It acts as a solvent and humectant to help dissolve active ingredients and maintain moisture in the formulation.
  • UNII LM6Q66468X
    A synthetic polymer made from polyethylene glycol and polypropylene glycol combined with dimethyl ether. Used as a solvent and humectant to help dissolve active ingredients and retain moisture in topical formulations.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII YPM0ZOC2HR
    A synthetic emulsifier derived from glycerin and castor oil. It helps mix oil and water-based ingredients together in the formulation to create a uniform product and improve texture.
  • UNII BI896CKT6B
    A plant extract from the tormentil root, used as a natural astringent and binding agent. It helps hold the medicine together and may provide texture or consistency to the formulation.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • 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 4VON5FNS3C
    Sodium metabisulfite is a preservative derived from sulfur compounds. It prevents microbial growth and oxidation in medicines, helping extend shelf life and maintain product stability.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • UNII LDC331P08E
    A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
  • UNII 25LXE464L2
    A silicone-based polymer used as a glidant and anti-caking agent in solid dosage forms. It reduces friction between particles and prevents clumping, helping powders flow smoothly during manufacturing and tablet compression.
  • 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.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.

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

The official label also statesDimethicone, Water, Zinc Oxide (nano), Alcohol, Diisopropyl Sebacate, Octocrylene, Isohexadecane, Ethylhexyl Salicylate, C12-15 Alkyl Benzoate, PEG/PPG-9/2 Dimethyl Ether, Zea Mays (Corn) Starch, Talc, Silica, Isopropyl Myristate, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Titanium Dioxide (nano), PEG-9 Polydimethylsiloxyethyl Dimethicone, Dextrin Palmitate, Glycerin, Homosalate, Ethylhexyl Triazone, Triethoxycaprylylsilane, Disteardimonium Hectorite, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, PEG-10 Dimethicone, Isostearic Acid, Polyglyceryl-6 Polyricinoleate, Sodium Chloride, Aluminum Hydroxide, Stearic Acid Other Trace Ingredients: EDTA Trisodium, PEG-6, Butylene Glycol, Fragrance (Parfum), Tocopherol (Vitamin E), BHT, Bis-Butyl Polydimethylsiloxane Polyglycerin-3, Sodium Metabisulfite, PEG/PPG-14/7 Dimethyl Ether, Trimethylsiloxysilicate, Panax Ginseng Root Extract, Dipotassium Glycyrrhizate, Camellia Sinensis Leaf Extract, Potentilla Erecta Root Extract, Citrus Unshiu Peel Extract, Synthetic Fluorphlogopite, Acetylated Sodium Hyaluronate, Lauryl Betaine, Soluble Collagen, Phenoxyethanol, Sodium Benzoate

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.

Manufacturer & labeler

LabelerHONGKONG JIAHE INTERNATIONAL HOLDING LIMITED
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code87719
First marketedJun 2026
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 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 9 words ▾

Stop use and ask a doctor if rash occurs.

⏱️ Dosage and Administration 96 words ▾

Directions apply generously and evenly 15 minutes before sun exposure reapply after80 minutes of swimming or sweating immediately after towel drying at least every 2 hours Sun Protection Measures Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sub and other sun protection measures including: Limit time in the sun, especially from 10 a.m.- 2 p.m. Wear long-sleeved shirts, pants, hats and sunglasses Children under 6 months: Ask a doctor

⚠️ Warnings 40 words ▾

Warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes Rinse with water to remove. If product is swallowed, get medical help or contact a Poison Control right away.

🧪 Active Ingredient 15 words ▾

Active Ingredients Purpose Zinc Oxide)： 10% Octocrylene)：8% Ethylhexyl Salicylate)： 4% Homosalate)： 8% Titanium Dioxide)： 3%

🧪 Inactive Ingredients 113 words ▾

Dimethicone, Water, Zinc Oxide (nano), Alcohol, Diisopropyl Sebacate, Octocrylene, Isohexadecane, Ethylhexyl Salicylate, C12-15 Alkyl Benzoate, PEG/PPG-9/2 Dimethyl Ether, Zea Mays (Corn) Starch, Talc, Silica, Isopropyl Myristate, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Titanium Dioxide (nano), PEG-9 Polydimethylsiloxyethyl Dimethicone, Dextrin Palmitate, Glycerin, Homosalate, Ethylhexyl Triazone, Triethoxycaprylylsilane, Disteardimonium Hectorite, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, PEG-10 Dimethicone, Isostearic Acid, Polyglyceryl-6 Polyricinoleate, Sodium Chloride, Aluminum Hydroxide, Stearic Acid Other Trace Ingredients: EDTA Trisodium, PEG-6, Butylene Glycol, Fragrance (Parfum), Tocopherol (Vitamin E), BHT, Bis-Butyl Polydimethylsiloxane Polyglycerin-3, Sodium Metabisulfite, PEG/PPG-14/7 Dimethyl Ether, Trimethylsiloxysilicate, Panax Ginseng Root Extract, Dipotassium Glycyrrhizate, Camellia Sinensis Leaf Extract, Potentilla Erecta Root Extract, Citrus Unshiu Peel Extract, Synthetic Fluorphlogopite, Acetylated Sodium Hyaluronate, Lauryl Betaine, Soluble Collagen, Phenoxyethanol, Sodium Benzoate

🎯 Purpose 30 words ▾

Uses - Helps prevent sunburn - If used as directed with other sun protection measures (see Directions), decreases the risk of skincancer and early skin aging caused by the sun

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 HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED 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.
← 87719-0001-01 · HONGKONG 87720-0202-21 · Lifeline →
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.