Home › NDC Lookup › Ingredients › Chop Saver Fresh Citrus Spf 15 Lip Balm › 83724-0770-01
AVOBENZONE,OCTINOXATE,OCTISALATE,OCTOCRYLENE Chop Saver Fresh Citrus SPF 15 Lip Balm 2 g/100g; 6.5 g/100g; 5 g/100g; 1.5 g/100g Stick, 1 tube — NDC 83724-0770-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

AVOBENZONE,OCTINOXATE,OCTISALATE,OCTOCRYLENE Chop Saver Fresh Citrus SPF 15 Lip Balm 2 g/100g; 6.5 g/100g; 5 g/100g; 1.5 g/100g Stick, 1 tube — NDC 83724-770-01 (Billing 83724-0770-01)

by Good for the Goose Products, LLC · 1 TUBE in 1 BLISTER PACK / 4.25 g in 1 TUBE

This is a package of 1 tube of AVOBENZONE,OCTINOXATE,OCTISALATE,OCTOCRYLENE Chop Saver Fresh Citrus SPF 15 Lip Balm 2 g/100g; 6.5 g/100g; 5 g/100g; 1.5 g/100g Stick from Good for the Goose Products, LLC, marketed since Oct 2023 and currently FDA-listed. It is this product's only package size.

NDC 83724-0770-01
🏷️ FDA NDC (as labeled) 83724-770-01 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 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 83724-770-01
Product NDC 83724-770
11-digit billing NDC 83724077001
UNII G63QQF2NOX, 4Y5P7MUD51, 4X49Y0596W, 5A68WGF6WM
UPC 0182740000028
Application # M020
SPL Set ID 2786cec8-0b8e-9c83-e063-6394a90ab338
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-10-15
Route TOPICAL
Dosage form STICK
Substance AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 83724-770-01 — 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 → 83724-0770-01. 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?

This is a lip balm stick marketed as an over-the-counter sunscreen product under FDA's monograph rules for sunscreen drugs. It contains four UV-filtering ingredients (avobenzone, octinoxate, octisalate, and octocrylene) that are commonly used together in sunscreen formulations to absorb or scatter ultraviolet light. The product is applied topically to the lips and is flavored with fresh citrus. This type of product is typically intended to help protect the lip area from sun exposure.

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 eachPer 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
83724-0770-01 You're viewing this Main listing 1 TUBE in 1 BLISTER PACK / 4.25 g in 1 TUBE 2023-10-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Avobenzone,Octinoxate,Octisalate,Octocrylene 2 g/100g; 6.5 g/100g; 5 g/100g; 1.5 g/100gthis 83724-0770-01 Good 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

🏛️
2023
On the market since
Oct 2023
📍
2026
Currently FDA-listed
3 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.

  • UNII H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • 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.
  • UNII 54JB35T06A
    A natural oil extracted from apricot pits, used as an emollient and lubricant in topical products. It helps soften the skin and improves the texture and spreadability of creams and lotions.
  • UNII O80TY208ZW
    Arnica montana is a plant extract used in some formulations as a flavoring agent or traditional botanical ingredient. It may contribute mild taste or aroma to the product.
  • UNII 6VNO72PFC1
    A natural oil extracted from avocado fruit. It's used in medicines as an emollient and carrier to help dissolve or deliver active ingredients and improve how the product feels on skin or mucous membranes.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • 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 R12CBM0EIZ
    A natural wax derived from a Brazilian palm tree, used as a coating and polish on tablets and capsules. It creates a smooth, shiny finish that protects the medicine and improves appearance.
  • UNII D5340Y2I9G
    Castor oil is a natural plant-based oil used in medicines as a lubricant, laxative agent, and solvent. It helps medicine ingredients dissolve or flow smoothly and can aid bowel movement in formulations designed for that purpose.
  • UNII DG4F8T839X
    A plant extract from comfrey leaves used as a natural ingredient in formulations. It may serve as a soothing agent or botanical additive in topical or oral preparations.
  • UNII SAS9Z1SVUK
    A natural oil extracted from ginger root that adds flavor and aroma to the medicine. It may also serve as a preservative or help mask unpleasant tastes in the formulation.
  • UNII 930MLC8XGG
    A plant oil extracted from grape seeds, used as an emollient and solvent in medicines. It helps dissolve active ingredients and improve the texture and absorption of topical or liquid formulations.
  • UNII YR377U58W9
    Grapefruit oil is a natural aromatic extract from grapefruit peel. It's used in medicines as a flavoring agent to improve taste and sometimes as a fragrance component.
  • UNII ET5GD00TRP
    A natural oil extracted from lemon peel used as a flavoring agent and fragrance in medicines. It masks bitter tastes and adds pleasant lemon flavor to make medications easier to take.
  • UNII 7937R189CB
    A natural oil extracted from Persian lime fruit, used as a flavoring agent to add citrus taste and aroma to medicines. It may also provide some antimicrobial properties in the formulation.
  • UNII 4OXD9M35X2
    A natural fat extracted from mango seeds, used as an emollient and binder to soften the medicine and help hold ingredients together in creams, lotions, and solid formulations.
  • UNII H4QNH2ZN7A
    Orange oil is a natural fragrant liquid extracted from orange peel. It's added to medicines as a flavoring agent to improve taste and mask bitter flavors, making the medicine more palatable to take.
  • UNII 7Q50F46595
    Pea protein is a plant-based powder extracted from peas. It's used as a binder and filler in tablets and capsules to hold ingredients together and add bulk to the formulation.
  • UNII 8O2V33JG64
    A plant extract from red raspberry leaves, used as a natural flavoring or coloring agent in medicines. It may also serve as a mild preservative or provide antioxidant properties to the formulation.
  • UNII V8UV0R324S
    A plant extract from white willow bark used as a natural flavoring agent and to provide mild astringent properties in some formulations.
  • 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 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.

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

The official label also statesInactive Ingredients: Castor Oil*, Candelilla Wax, Beeswax*, Aloe Vera*, Calendula*, Comfrey*, Raspberry Leaf*, Willow Bark*, Ginger Root*, Shea Butter*, Mango Butter*, Carnauba Wax*, Avocado Oil*, Arnica Extract, Lemon Essential Oil*, Vitamin E, Grapefruit Essential Oil, Orange Essential Oil*, Lime Essential Oil*, Ginger Essential Oil*, Pea Isolate *Certified Organic Ingredient

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

LabelerGood for the Goose Products, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code83724
First marketedOct 2023
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.

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Recent Major Changes 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 4 words ▾

Use: Helps prevent sunburn

⏱️ Dosage and Administration 87 words ▾

Directions: apply liberally 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10am-2pm. wear long-sleeved shirts, pants, hats and sunglasses children under 6 months of age: ask a doctor

⚠️ Warnings 32 words ▾

Warnings: Do not use on damaged or broken skin When using this product, keep out of eyes Stop use and ask a doctor if rash occurs Keep out of reach of children.

📦 Storage and Handling 11 words ▾

Other information: Protect this product from excessive heat and direct sun

🧪 Active Ingredient 10 words ▾

Active Ingredients: Avobenzone 2%, Octinoxate 6.5% Octisalate 5%, Octocrylene 1.5%

🧪 Inactive Ingredients 49 words ▾

Inactive Ingredients: Castor Oil*, Candelilla Wax, Beeswax*, Aloe Vera*, Calendula*, Comfrey*, Raspberry Leaf*, Willow Bark*, Ginger Root*, Shea Butter*, Mango Butter*, Carnauba Wax*, Avocado Oil*, Arnica Extract, Lemon Essential Oil*, Vitamin E, Grapefruit Essential Oil, Orange Essential Oil*, Lime Essential Oil*, Ginger Essential Oil*, Pea Isolate *Certified Organic Ingredient

🎯 Purpose 2 words ▾

Purpose: Sunscreen

📄 Do Not Use 8 words ▾

Do not use on damaged or broken skin

📄 When Using This Product 8 words ▾

When using this product, keep out of eyes

📄 Stop Use and Ask a Doctor If 9 words ▾

Stop use and ask a doctor if rash occurs

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Questions or Comments 4 words ▾

Questions or comments? 877-346-0951

📄 Recent Major Changes 94 words ▾

Dosage and Administration section updated to read: Directions: apply liberally 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10am-2pm. wear long-sleeved shirts, pants, hats and sunglasses children under 6 months of age: ask a doctor

📄 Package Label / Principal Display Panel 33 words ▾

Blister Card artwork Chop Saver Lip Care Broad Spectrum SPF 15 Sunscreen Lip Balm Blister Card Artwork

Tube Label Artwork Chop Saver Lip Care Broad Spectrum SPF 15 Sunscreen Lip Balm Label Artwork

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 Good for the Goose Products, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Good for the Goose Products, LLC 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.
← 83723-0010-50 · Botanix 83727-0294-00 · Skin →
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.