Home › NDC Lookup › Ingredients › Hydrating Tinted Moisturizer Spf50 › 87508-0224-01
HYDRATING TINTED MOISTURIZER SPF50 6 g/1001; 5.38 g/1001; 4 g/1001 Cream, 5 bottles — NDC 87508-0224-01 package photo

HYDRATING TINTED MOISTURIZER SPF50 6 g/1001; 5.38 g/1001; 4 g/1001 Cream, 5 bottles

by NING PTE. LTD. · 5 BOTTLE in 1 BOX (87508-224-01) / 1 CREAM in 1 BOTTLE
NDC 87508-0224-01
🏷️ FDA NDC (as labeled) 87508-224-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

FDA NDC (as labeled) 87508-224-01
Product NDC 87508-224
11-digit billing NDC 87508022401
UNII 4Y5P7MUD51, 15FIX9V2JP, 5A68WGF6WM
SPL Set ID 4cf8d3d3-eebf-2da0-e063-6294a90a7065
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-14
Route CUTANEOUS
Dosage form CREAM
Substance OCTINOXATE; TITANIUM DIOXIDE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 87508-224-01 — 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 → 87508-0224-01. 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.

🏭 Manufacturer & labeler

LabelerNING PTE. LTD.
Labeler code87508
First marketedMar 2026
Product typeHuman Otc Drug
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 an unapproved homeopathic cream applied to the skin. It contains three ingredients typically used as UV filters in sunscreen products: octinoxate, octocrylene, and titanium dioxide. Homeopathic products are marketed based on homeopathic tradition and principles rather than being evaluated by the FDA for safety or effectiveness. This product's claims and benefits are not established through standard medical or scientific review.

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 6MW60CB71P
    A stabilized form of vitamin C used as an antioxidant in medicines. It prevents other ingredients from breaking down or discoloring during storage.
  • 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 W59H9296ZG
    A synthetic polymer made from acrylic compounds and vinylpyrrolidone. It works as a film-former and thickener in topical products, helping create a smooth texture and improve how the medication spreads on skin.
  • UNII 3SCV180C9W
    Betaine is a naturally occurring organic compound found in plants and animals. In medicines, it acts as an osmoprotectant and stabilizer, helping maintain the product's moisture balance and preserve its chemical stability during storage.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • 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 E4F12ROE70
    A refined mineral oil derived from crude petroleum containing 13 to 14 carbon chains. It acts as a solvent, emollient, and carrier in topical formulations to help dissolve active ingredients and improve product texture and spreadability.
  • UNII XHK3U310BA
    Cyclohexasiloxane is a silicon-based liquid that acts as a solvent and conditioning agent in medicines. It helps dissolve or carry other ingredients and improves how the product spreads or feels on the skin.
  • UNII 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • UNII 9H4PO4Z4FT
    A sulfur-containing organic compound used as a solvent and penetration enhancer in medicines. It helps dissolve active ingredients and improve their absorption through skin or mucous membranes.
  • UNII I6KB4GE3K4
    A synthetic oil derived from petrochemicals, used as an emollient and solvent in topical formulations. It helps dissolve active ingredients and improve the texture and spreadability of creams, lotions, and ointments.
  • 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 G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII B697894SGQ
    Polyethylene glycol 400 is a clear, thick liquid made from petroleum-derived polymers. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII E2KR9C9V2I
    Polyacrylamide is a synthetic polymer used as a thickening agent and binder in medications. It helps create the proper texture and hold ingredients together in the formulation.
  • UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII GW89575KF9
    Squalane is a lightweight oil derived from plant sources or synthesized. It acts as an emollient and lubricant in formulations, helping ingredients blend smoothly and improving product texture and spreadability.
  • UNII M96W2OLL2V
    A synthetic cleaning agent derived from lauryl alcohol. In medicines, it acts as a surfactant and emulsifier to help mix oil and water-based ingredients and improve product texture and stability.
  • UNII KFR5QEN0N9
    A synthetic plastic polymer that helps form a protective film coating on the medicine. It's used as a binder and film-former to hold the tablet or capsule together and control how quickly the drug dissolves.
  • 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.

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

The official label also statesWater,Glycerin,Ethylhexyl Methoxycinnamate,Ethylhexyl Isononanoate,Titanium Dioxide,Cyclopentasiloxane,CI 77891,Ammonium Acryloyldimethyltaurate/VP Copolymer,Polyamino Sugar Condensate,Cyclohexasiloxane,Trilaureth-4 Phosphate,Polyacrylamide,Hydroxyacetophenone,Dimethyl Sulfone,Yeast Polysaccharides,Peg-8,C13-14 Isoparaffin,Propanediol,Betaine,VP/Hexadecene Copolymer,Silica,Aluminum Hydroxide,Tocopheryl Acetate,Butylene Glycol,Niacinamide,Bifida Ferment Filtrate,Centella Asiatica Leaf Extract,Aloe Barbadensis Leaf Extract,3-o-Ethyl Ascorbic Acid,Bisabolol,Squalane,Tranexamic Acid,Tremella Fuciformis Sporocarp Extract,Dimethicone,Polyglyceryl-10 Laurate,Polyglyceryl-10 Myristate,Polyglyceryl-3 Distearate,1,2-Hexanediol,Pentylene Glycol,Polyglyceryl-2 Triisostearate,Laureth-7,C13-16 Isoparaffin,Caprylhydroxamic Acid,Stearic Acid,Proline,Avena Sativa (Oat) Kernel Extract,Citric Acid,Panthenol,Isostearyl Alcohol,Paeonia Albiflora Root Extract,Centella Asiatica Extract,Ceramide NP,Polygonum Cuspidatum Root Extract,Scutellaria Baicalensis Root Extract,Portulaca Oleracea Extract,Camellia Sinensis Leaf Extract,Glycyrrhiza Glabra (Licorice) Root Extract,Sodium Acetylated Hyaluronate,Sodium Hyaluronate,Rosmarinus Officinalis (Rosemary) Leaf Extract,Chamomilla Recutita (Matricaria) Flower Extract,Sodium Hyaluronate Crosspolymer,Hydrolyzed Sodium Hyaluronate,Ethylhexylglycerin,Fragrance

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 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Hydrating Tinted Moisturizer Spf50 6 g/1001; 5.38 g/1001; 4 g/1001this 87508-0224-01 NING 5 bottles — — 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
Mar 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
87508-0224-01 You're viewing this 5 BOTTLE in 1 BOX (87508-224-01) / 1 CREAM in 1 BOTTLE 2026-03-14 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

HYDRATING TINTED MOISTURIZER SPF50 6 g/1001; 5.38 g/1001; 4 g/1001 CREAM is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

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 "Unapproved Homeopathic". 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 FDA registers it as 87508-224-01, 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: 87508-0224-01, written without dashes as 87508022401. 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 87508-0224-01, the first segment (87508) is the labeler code FDA assigned to NING PTE. LTD.; the middle segment (0224) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
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 NING PTE. LTD.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
NING PTE. LTD. 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 28 words ▾

After cleansing your skin, apply an appropriate amount of this product evenly to the face or neck and gently massage your skin until this product is fully absorbed.

⏱️ Dosage and Administration 6 words ▾

NET WT.

1.76OZ. / 50G

⚠️ Warnings 19 words ▾

In case of contact with eyes, rinse immediately with water. Stop using immediately if there are any allergy reactions.

🧪 Active Ingredient 2 words ▾

Octinoxate,Octocrylene,Titanium Dioxide

🧪 Inactive Ingredients 81 words ▾

Water,Glycerin,Ethylhexyl Methoxycinnamate,Ethylhexyl Isononanoate,Titanium Dioxide,Cyclopentasiloxane,CI 77891,Ammonium Acryloyldimethyltaurate/VP Copolymer,Polyamino Sugar Condensate,Cyclohexasiloxane,Trilaureth-4 Phosphate,Polyacrylamide,Hydroxyacetophenone,Dimethyl Sulfone,Yeast Polysaccharides,Peg-8,C13-14 Isoparaffin,Propanediol,Betaine,VP/Hexadecene Copolymer,Silica,Aluminum Hydroxide,Tocopheryl Acetate,Butylene Glycol,Niacinamide,Bifida Ferment Filtrate,Centella Asiatica Leaf Extract,Aloe Barbadensis Leaf Extract,3-o-Ethyl Ascorbic Acid,Bisabolol,Squalane,Tranexamic Acid,Tremella Fuciformis Sporocarp Extract,Dimethicone,Polyglyceryl-10 Laurate,Polyglyceryl-10 Myristate,Polyglyceryl-3 Distearate,1,2-Hexanediol,Pentylene Glycol,Polyglyceryl-2 Triisostearate,Laureth-7,C13-16 Isoparaffin,Caprylhydroxamic Acid,Stearic Acid,Proline,Avena Sativa (Oat) Kernel Extract,Citric Acid,Panthenol,Isostearyl Alcohol,Paeonia Albiflora Root Extract,Centella Asiatica Extract,Ceramide NP,Polygonum Cuspidatum Root Extract,Scutellaria Baicalensis Root Extract,Portulaca Oleracea Extract,Camellia Sinensis Leaf Extract,Glycyrrhiza Glabra (Licorice) Root Extract,Sodium Acetylated Hyaluronate,Sodium Hyaluronate,Rosmarinus Officinalis (Rosemary) Leaf Extract,Chamomilla Recutita (Matricaria) Flower Extract,Sodium Hyaluronate Crosspolymer,Hydrolyzed Sodium Hyaluronate,Ethylhexylglycerin,Fragrance

🎯 Purpose 28 words ▾

After cleansing your skin, apply an appropriate amount of this product evenly to the face or neck and gently massage your skin until this product is fully absorbed.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87507-0002-02 · Forest 87509-0001-06 · Famora →
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.