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Glow Gloss Lip Balm SPF 40 Strawberry Popsicle Homosalate, Octocrylene, Avobenzone, Octisalate 5 g/100mL; 4.5 g/100mL; 3 g/100mL; 4 g/100mL Gel — NDC 75936-0646-02 package photo

Glow Gloss Lip Balm SPF 40 Strawberry Popsicle Homosalate, Octocrylene, Avobenzone, Octisalate 5 g/100mL; 4.5 g/100mL; 3 g/100mL; 4 g/100mL Gel

by Supergoop! · 1 TUBE in 1 BOX (75936-646-02) / 15 mL in 1 TUBE (75936-646-01)
NDC 75936-0646-02
🏷️ FDA NDC (as labeled) 75936-646-02 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 10, 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) 75936-646-02
Product NDC 75936-646
11-digit billing NDC 75936064602
UNII 5A68WGF6WM, V06SV4M95S, 4X49Y0596W, G63QQF2NOX
Application # M020
SPL Set ID 26d2897f-46a7-52b2-e063-6394a90aed32
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-11-13
Route TOPICAL
Dosage form GEL
Substance HOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
Why two NDCs? The FDA registers this code as 75936-646-02 — 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 → 75936-0646-02. 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

LabelerSupergoop!
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code75936
First marketedNov 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.

🩺 Clinical

🧪 What is this product?

Glow Gloss Lip Balm SPF 40 is a topical gel product marketed as an over-the-counter sunscreen under FDA's monograph rules. It contains four UV-filtering ingredients (homosalate, octocrylene, avobenzone, and octisalate) that are typically used together to absorb and scatter ultraviolet light from the sun. This type of lip balm is commonly used to help protect the lips from sun exposure. The product is formulated as a glossy gel applied directly to the lips.

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 36HQN158VC
    Alpha-bisabolol is a naturally derived oily liquid from plant sources. It works as a fragrance, flavor, and skin-conditioning agent in topical medicines and cosmetic products.
  • UNII XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • 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.
  • UNII WW4FVB2PEM
    A waxy compound made from fatty acids, used as an emulsifier and thickener to help blend oil and water ingredients together and give the medicine a smooth, stable texture.
  • UNII 9M64UO4C25
    A synthetic oily substance used as an emollient and texture enhancer in medicines. It helps soften formulations, improves how the medicine spreads or feels on skin, and can act as a lubricant in tablets or capsules.
  • 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.
  • 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.
  • UNII 2LRS185U6K
    D&C Red No. 27 is a synthetic red colorant used in medicines and cosmetics. It gives tablets, capsules, or liquids their red or reddish color so products are visually identifiable.
  • UNII WL0328HX19
    A natural plant-based wax derived from candelilla shrub leaves. It acts as a coating agent, hardener, and texture modifier to control how quickly the medicine releases and to improve the tablet or capsule's appearance and stability.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • UNII 4YI0729529
    A synthetic oil made from plant-derived hydrocarbons that has been chemically saturated. It acts as a lubricant and glidant to help the medicine flow smoothly during manufacturing and improve tablet handling.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • UNII 461N1O614Y
    A synthetic oily liquid used as an emollient and solvent in medications. It helps dissolve active ingredients and improves how the medicine spreads or absorbs through the skin.
  • UNII T7A529FB8O
    A synthetic compound derived from amino acids and palmitic acid, used as a skin-conditioning agent or emollient in topical formulations to help soften and protect the skin surface.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • UNII 255PIF62MS
    A synthetic antioxidant compound used to prevent oils and fats in medications from breaking down or becoming rancid during storage. It helps maintain the medicine's stability and shelf life.
  • UNII II29C6E5R3
    A plant-derived ingredient from the pigweed species. It acts as a natural binder and thickener to help hold the medication's components together and improve texture and consistency.
  • UNII 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • UNII 01S2G2C1E4
    Sorbitan isostearate is an emulsifier derived from sorbitol and isostearic acid. It helps mix oil and water-based ingredients together and keeps them blended throughout the medicine's shelf life.
  • 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.
  • UNII 4J2TY8Y81V
    A natural flavoring derived from strawberries that gives the medicine its strawberry taste and smell. It helps make the medicine more pleasant to take, especially for children.
  • UNII H58HX2GWJ5
    A synthetic rubber made from styrene and isoprene monomers. It serves as a film-former and binder in tablet coatings and sustained-release formulations to control how quickly the medicine dissolves and releases.
  • UNII 3H18P0UK73
    Sucrose cocoate is a natural emulsifier made from coconut oil and sugar. It helps blend water and oil-based ingredients together in formulations.
  • UNII 50XT325OOH
    A synthetic ester derived from citric acid and fatty alcohols. It acts as a plasticizer and emollient in the medicine, helping soften and improve the flexibility of coatings and formulations.

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

The official label also statesInactive Ingredients: Hydrogenated Poly(C6-14 Olefin), Ethylene/Propylene/Styrene Copolymer, Butyloctyl Salicylate, C18-38 Alkyl Hydroxystearoyl Stearate, Euphorbia Cerifera (Candelilla) Wax, Synthetic Wax, Flavor, Triisostearyl Citrate, Octyldodecanol, Tocopherol, Cocos Nucifera (Coconut) Oil, Butyrospermum Parkii (Shea) Butter, Simmondsia Chinensis (Jojoba) Seed Oil, Stevia Rebaudiana Leaf/Stem Extract, Portulaca Pilosa Extract, Citric Acid, Bisabolol, Sorbitan Isostearate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sucrose Cocoate, Sorbitan Oleate, Palmitoyl Tripeptide-38, Butylene/Ethylene/Styrene Copolymer, Cetearyl Ethylhexanoate. May Contain: Titanium Dioxide, Red 28 Lake, Iron Oxides, Red 7 Lake, Yellow 5 Lake.

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
Glow Gloss Lip Balm SPF 40 Pink Peppermint 5 g/100mL; 4.5 g/100mL; 3 g/100mL; 4 g/100mL 75936-0645-02 Supergoop! 1 tube — — FDA listed —
Glow Gloss Lip Balm SPF 40 Strawberry Popsicle 5 g/100mL; 4.5 g/100mL; 3 g/100mL; 4 g/100mLthis 75936-0646-02 Supergoop! 1 tube — — FDA listed —
Glow Gloss Lip Balm SPF 40 Caramel Glaze 5 g/100mL; 4.5 g/100mL; 3 g/100mL; 4 g/100mL 75936-0669-02 Supergoop! 1 tube — — FDA listed —
Glow Gloss Lip Balm SPF 40 Vanilla Soft Serve 5 g/100mL; 4.5 g/100mL; 3 g/100mL; 4 g/100mL 75936-0644-02 Supergoop! 1 tube — — 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

🏛️
2024
On the market since
Nov 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
75936-0646-02 You're viewing this 1 TUBE in 1 BOX (75936-646-02) / 15 mL in 1 TUBE (75936-646-01) 2024-11-15 Active

🧭 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 FDA registers it as 75936-646-02, 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: 75936-0646-02, written without dashes as 75936064602. 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 75936-0646-02, the first segment (75936) is the labeler code FDA assigned to Supergoop!; the middle segment (0646) 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.
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 Supergoop!. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Supergoop! 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 9 words ▾

Stop use and ask a doctor if rash occurs.

⏱️ Dosage and Administration 101 words ▾

• apply generously and evenly 15 minutes before sun exposure • reapply at least every 2 hours • use a water resistant sunscreen if swimming or sweating • 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 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 of age: Ask a doctor

⚠️ Warnings 28 words ▾

• 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.

🧪 Active Ingredient 8 words ▾

Avobenzone 3%, Homosalate 5%, Octisalate 4%, Octocrylene 4.5%

🧪 Inactive Ingredients 77 words ▾

Inactive Ingredients: Hydrogenated Poly(C6-14 Olefin), Ethylene/Propylene/Styrene Copolymer, Butyloctyl Salicylate, C18-38 Alkyl Hydroxystearoyl Stearate, Euphorbia Cerifera (Candelilla) Wax, Synthetic Wax, Flavor, Triisostearyl Citrate, Octyldodecanol, Tocopherol, Cocos Nucifera (Coconut) Oil, Butyrospermum Parkii (Shea) Butter, Simmondsia Chinensis (Jojoba) Seed Oil, Stevia Rebaudiana Leaf/Stem Extract, Portulaca Pilosa Extract, Citric Acid, Bisabolol, Sorbitan Isostearate, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Sucrose Cocoate, Sorbitan Oleate, Palmitoyl Tripeptide-38, Butylene/Ethylene/Styrene Copolymer, Cetearyl Ethylhexanoate.

May Contain: Titanium Dioxide, Red 28 Lake, Iron Oxides, Red 7 Lake, Yellow 5 Lake.

🎯 Purpose 30 words ▾

• Helps prevent sunburn. • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer 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 ↗
← 75936-0645-02 · Supergoop! 75936-0647-01 · Supergoop, →
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.