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Birdie Glow Tinted Glow Moisturizer SPF 30 2.7 g/100mL; 4.8 g/100mL; 5 g/100mL; 4.6 g/100mL; 9 g/100mL Lotion, 100 mL — NDC 84222-003-01 (Billing 84222-0003-01)

by Foshan Miwei Cosmetics Co., Ltd. · 100 mL in 1 BOTTLE

This is a package of 100 mL of Birdie Glow Tinted Glow Moisturizer SPF 30 2.7 g/100mL; 4.8 g/100mL; 5 g/100mL; 4.6 g/100mL; 9 g/100mL Lotion from Foshan Miwei Cosmetics Co., Ltd., no longer marketed (first marketed Sep 2024), no longer in the FDA NDC Directory. It is this product's only package size.

NDC 84222-0003-01
🏷️ FDA NDC (as labeled) 84222-003-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Inactivated by FDA ⇄ Compare with another NDC
🗂️ 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 →

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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84222-003-01
Product NDC 84222-003
11-digit billing NDC 84222000301
UNII G63QQF2NOX, 5A68WGF6WM, V06SV4M95S, 4X49Y0596W, 4Y5P7MUD51
Application # M020
SPL Set ID 22745ac1-3322-7be9-e063-6294a90ae014
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2024-09-20
Route TOPICAL
Dosage form LOTION
Substance AVOBENZONE; OCTOCRYLENE; HOMOSALATE; ETHYLHEXYL SALICYLATE; OCTINOXATE
Why two NDCs? The FDA registers this code as 84222-003-01 — 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 → 84222-0003-01. 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?

Birdie Glow Tinted Glow Moisturizer SPF 30 is a topical lotion marketed as an over-the-counter sunscreen product under FDA's OTC monograph rules. It contains five active ingredients that function as ultraviolet light filters: avobenzone, ethylhexyl salicylate, homosalate, octinoxate, and octocrylene. These ingredients are commonly used together in sunscreen formulations to help absorb and scatter UV radiation from the sun. The product is applied to the skin and also contains tinting and moisturizing components.

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
84222-0003-01 You're viewing this Main listing 100 mL in 1 BOTTLE 2024-09-20 — Inactivated by FDA

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Birdie Glow Tinted Glow Moisturizer SPF 30 2.7 g/100mL; 4.8 g/100mL; 5 g/100mL; 4.6 g/100mL; 9 g/100mLthis 84222-0003-01 Foshan 100 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

🏛️
2024
On the market since
Sep 2024
📍
2026
Currently FDA-listed
2 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.

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.

  • 1 mL / 100 mL UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • 0.5 mL / 100 mL UNII TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • 0.2 mL / 100 mL UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • 0.3 mL / 100 mL 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.
  • 0.0046 mL / 100 mL 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.
  • 2 mL / 100 mL UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • 0.0135 mL / 100 mL UNII 035JKJ76MT
    A silicone-based ingredient that helps oil and water mix together in formulations. It works as an emulsifier to create smooth, stable textures in topical medicines and creams.
  • 0.37 mL / 100 mL UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • 0.162 mL / 100 mL UNII EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • 0.07 mL / 100 mL UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • 1.95 mL / 100 mL UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • 0.2 mL / 100 mL UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • 0.0063 mL / 100 mL 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.
  • 0.05 mL / 100 mL UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • 5 mL / 100 mL 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.
  • 0.5 mL / 100 mL 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.
  • 0.1435 mL / 100 mL UNII S4V5BS6GCX
    A synthetic oily liquid used as an emollient and solvent in topical medications. It helps dissolve active ingredients and creates a smooth, spreadable texture on the skin.
  • 0.1125 mL / 100 mL UNII N6K5787QVP
    Light mineral oil is a clear, odorless liquid derived from petroleum. In medicines, it acts as a lubricant and emollient to help the product spread smoothly and improve texture.
  • 0.85 mL / 100 mL 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.
  • 0.002 mL / 100 mL UNII 39DK5WQ2PR
    A synthetic polymer made from methacrylate, methoxy polyethylene glycol, maleate, and styrene. It's used as a coating or binder to control how quickly the medicine dissolves and releases its active ingredients in the body.
  • 1.8 mL / 100 mL UNII V8A1AW0880
    Mica is a naturally occurring mineral that's ground into fine powder. It's used in medicines as a colorant and anti-caking agent to improve appearance and prevent clumping in tablets or powders.
  • 0.06 mL / 100 mL UNII 3D47Q6D93C
    A synthetic ester derived from fatty acids, used as an emollient and lubricant in topical formulations. It helps soften the skin and improves the texture and spreadability of creams and ointments.
  • 0.24 mL / 100 mL UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • 2 mL / 100 mL UNII 46P231IQV8
    A synthetic emulsifier derived from glycerin and fatty acids. It helps blend oil and water-based ingredients together in cosmetic and pharmaceutical formulations to create stable, uniform products.
  • 2.7 mL / 100 mL UNII 4T2L7QI313
    A waxy, plant-derived thickener made from glycerol and behenic acid. It's used as an emulsifier and stabilizer to help blend oil and water-based ingredients together and maintain texture in creams and lotions.
  • 0.0185 mL / 100 mL UNII YXH47AOU0F
    A synthetic fatty acid used as a thickener and stabilizer in medicines. It helps create the right texture and prevents separation of ingredients in liquid or semi-solid formulations.
  • 2 mL / 100 mL UNII CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • 0.0014 mL / 100 mL UNII 8D08K3S51E
    Propylene carbonate is a clear liquid solvent derived from propylene. It helps dissolve or suspend active ingredients in liquid medicines and can improve how well the product flows and mixes.
  • 0.1 mL / 100 mL UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • 0.1 mL / 100 mL UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • 0.27 mL / 100 mL UNII 285CYO341L
    Sodium polyacrylate is a synthetic polymer that absorbs and holds water. In medicines, it acts as a disintegrant, helping tablets break apart quickly in the stomach, and as a binder, holding tablet ingredients together.
  • 0.0225 mL / 100 mL UNII 06XEA2VD56
    Sorbitan oleate is an emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in the medicine.
  • 0.1 mL / 100 mL UNII KM7N50LOS6
    Tin oxide is an inorganic mineral compound used in medicines as a colorant and opacifying agent. It provides white or off-white color to tablets, capsules, and coatings while helping make formulations less transparent.
  • 0.0225 mL / 100 mL UNII X9HD79I514
    A synthetic liquid cleansing agent made from plant oils and ethylene oxide. It helps dissolve and mix oil and water-based ingredients together in the medicine, acting as an emulsifier and solubilizer.
  • 0.0228 mL / 100 mL 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.
  • 51.0125 mL / 100 mL 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.

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

The official label also statesWater, Glycerin, Macadamia Seed Oil Polyglyceryl-6 Esters Behenate, Cetearyl Alcohol, Polyglyceryl-3 Diisostearate, Polysorbate 60, CI 77891, Mica, Tocopheryl Acetate, Synthetic Fluorphlogopite, Hydroxyacetophenone, 1,2-Hexanediol, CI 77491, Ammonium Acryloyldimethyltaurate/VP Copolymer, Ammonium Polyacrylate, Paraffinum Liquidum, Aloe Barbadensis Leaf Water, Cocos Nucifera (Coconut) Oil, CI 77492, Isononyl Isononanoate, Mineral Oil, Butyrospermum Parkii (Shea) Butter, Sodium Hyaluronate, Tin Oxide, CI 77499, Octyldodecyl Stearoyl Stearate, Disodium EDTA, Triethoxycaprylylsilane, Sorbitan Oleate, Trideceth-9, Polyhydroxystearic Acid, Cetyl PEG/PPG-10/1 Dimethicone, Disteardimonium Hectorite, BHT, Styrene/Butadiene Copolymer, Propylene Carbonate

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

LabelerFoshan Miwei Cosmetics Co., Ltd.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code84222
First marketedSep 2024
Product typeHuman Otc Drug
Portfolio4 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 📋 Description 📄 Keep Out of Reach of Children 📄 Other Information 📄 Recent Major Changes 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 25 words ▾

Uses Helps prevent sunburn, decreases the risk of skin cancer and early skin aging if used as directed. SPF protection Perfect for all skin types

⏱️ Dosage and Administration 29 words ▾

Apply liberally 15 minutes before sun exposure; reapply at least every 2 hours; use a water-resis- tant sunscreen if swimming or sweating; children under 6 months: ask a doctor.

⚠️ Warnings 43 words ▾

Warnings · For external use only. · Do not use on damaged skin. · Avoid contact with eyes. Rinse with water if needed. · Stop use if rash occurs. · Keep out of reach of children. In case of ingestion, get medical help.

🧪 Active Ingredient 13 words ▾

Octocrylene 9% Homosalate 5% Ethylhexyl Salicylate 4.8% Ethylhexyl Methoxycinnamate 4.5954%. Butyl Methoxydibenzoylmethane 2.7%

🧪 Inactive Ingredients 77 words ▾

Water, Glycerin, Macadamia Seed Oil Polyglyceryl-6 Esters Behenate, Cetearyl Alcohol, Polyglyceryl-3 Diisostearate, Polysorbate 60, CI 77891, Mica, Tocopheryl Acetate, Synthetic Fluorphlogopite, Hydroxyacetophenone, 1,2-Hexanediol, CI 77491, Ammonium Acryloyldimethyltaurate/VP Copolymer, Ammonium Polyacrylate, Paraffinum Liquidum, Aloe Barbadensis Leaf Water, Cocos Nucifera (Coconut) Oil, CI 77492, Isononyl Isononanoate, Mineral Oil, Butyrospermum Parkii (Shea) Butter, Sodium Hyaluronate, Tin Oxide, CI 77499, Octyldodecyl Stearoyl Stearate, Disodium EDTA, Triethoxycaprylylsilane, Sorbitan Oleate, Trideceth-9, Polyhydroxystearic Acid, Cetyl PEG/PPG-10/1 Dimethicone, Disteardimonium Hectorite, BHT, Styrene/Butadiene Copolymer, Propylene Carbonate

🎯 Purpose 1 words ▾

Sunscreen

📋 Description 36 words ▾

Achieve a radiant, sun-kissed look with our Birdie Glow Fore Face Tinted Glow SPF Moisturizer. This lightweight formula provides a sheer tint while protecting your skin with SPF, making it perfect for your daily skincare routine.

📄 Keep Out of Reach of Children 14 words ▾

· Keep out of reach of children. In case of ingestion, get medical help.

📄 Other Information 12 words ▾

Other information · Protect this product from excessive heat and direct sun.

📄 Recent Major Changes 26 words ▾

Indications & Usage Updated indication wording for clarity (no change in therapeutic intent). Dosage and Administration Updated direction wording for clarity (no change in therapeutic intent).

📄 Package Label / Principal Display Panel 3 words ▾

box and label

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 No longer marketed (per FDA listing data)
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 "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.
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 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.
Who lists this product with the FDA?
Foshan Miwei Cosmetics Co., 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.
← 84222-0002-01 · Foshan 84222-0004-01 · Foshan →
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.