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Carmex Weather Guard Moisturizing Lip Balm SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM 30 mg/g; 100 mg/g; 50 mg/g; 90 mg/g; 310 mg/g Salve, 2 cylinders — NDC 10210-0056-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Carmex Weather Guard Moisturizing Lip Balm SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM 30 mg/g; 100 mg/g; 50 mg/g; 90 mg/g; 310 mg/g Salve, 2 cylinders — NDC 10210-0056-2 (Billing 10210-0056-02)

by Carma Laboratories, Inc. · 2 CYLINDER in 1 TRAY / 4.25 g in 1 CYLINDER

This is a package of 2 cylinders of Carmex Weather Guard Moisturizing Lip Balm SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM 30 mg/g; 100 mg/g; 50 mg/g; 90 mg/g; 310 mg/g Salve from Carma Laboratories, Inc., marketed since Feb 2023 and currently FDA-listed.

NDC 10210-0056-02
🏷️ FDA NDC (as labeled) 10210-0056-2 billing pads the package segment with a zero
This package
Contains2 cylinders Pack sizes2 compare ↓
Product page 10210-0056-01 Also comes in: 4.25 g 10210-0056-1
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

NDC database record

One package, one record: these facts belong to NDC 10210-0056-2 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
10210 labeler · 0056 product · 2 package
Package marketed since
Feb 23, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0083078113148
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 10210-0056-2
Product NDC 10210-0056
11-digit billing NDC 10210005602
UNII G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM, B6E5W8RQJ4
UPC 0083078113148
Application # M020
SPL Set ID 843677f2-78fa-4f3d-9fe6-e45e35b728e3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-02-23
Route TOPICAL
Dosage form SALVE
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; WHITE PETROLATUM
Why two NDCs? The FDA registers this code as 10210-0056-2 — a 5-4-1 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 package segment → 10210-0056-02. 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.

Clinical

🧪 What is this product?

This is an over-the-counter lip balm salve marketed under FDA's established category rules for sunscreen products. It contains four ultraviolet (UV) light-absorbing chemicals (avobenzone, homosalate, octisalate, and octocrylene) that are typically included in sunscreen formulations to help protect skin from sun exposure, plus white petrolatum, a moisturizing base ingredient commonly found in lip balms. The product is applied topically to the lips and is labeled with SPF 30, indicating its sun protection strength rating in that category.

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.
Try another pack size: 4.25 g
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
10210-0056-01 10210-0056-1 Main listing 1 CYLINDER in 1 CARTON / 4.25 g in 1 CYLINDER 2023-06-22 — Active
10210-0056-02 You're viewing this 2 CYLINDER in 1 TRAY / 4.25 g in 1 CYLINDER 2023-02-23 — Active

Pack size FAQ

What quantity is in this package?
This package contains 2 cylinders — 2 cylinder in 1 tray / 4.25 g in 1 cylinder.
How does this package differ from NDC 10210-0056-01?
Both are Carmex Weather Guard Moisturizing Lip Balm SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM 30 mg/g; 100 mg/g; 50 mg/g; 90 mg/g; 310 mg/g Salve — the drug itself is identical. This page's package is the 2 cylinders one, while NDC 10210-0056-01 is the 1 cylinder package.
What NDC number is used to bill for this package of Carmex Weather Guard Moisturizing Lip Balm SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM 30 mg/g; 100 mg/g; 50 mg/g; 90 mg/g; 310 mg/g Salve?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Carmex Weather Guard Moisturizing Lip Balm SPF 30 30 mg/g; 100 mg/g; 50 mg/g; 90 mg/g; 310 mg/gthis 10210-0056-02 Carma 2 cylinders — — 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
Feb 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 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 D072FFP9GU
    Cetyl esters wax is a waxy substance made from natural or synthetic fatty acids. It's used as a binder, hardening agent, and coating material to give tablets and capsules their structure and texture.
  • UNII 512OYT1CRR
    Cocoa butter is a natural fat extracted from cocoa beans. It's used in medicines as a base for suppositories and as a lubricant to help pills dissolve smoothly.
  • UNII 7EV65EAW6H
    Lanolin is a waxy substance derived from sheep's wool. It's used in medicines as an emollient and skin-conditioning agent to soften formulations and improve spreadability in topical products like creams and ointments.
  • UNII 412ZHA4T4Y
    A plant-derived oil extracted from meadowfoam seeds. It acts as an emollient and skin-conditioning agent, helping soften and smooth the product texture while improving how it spreads on skin.
  • 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 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.

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

The official label also stateseuphorbia cerifera (candelilla) wax, ozokerite, flavor, paraffin, beeswax, theobroma cacao (cocoa) seed butter, cetyl esters, lanolin, limnanthes alba (meadowfoam) seed oil, stevia rebaudiana extract

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

LabelerCarma Laboratories, Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code10210
First marketedFeb 2023
Product typeHuman Otc Drug
Portfolio56 products on file

More NDCs from Carma Laboratories, Inc. labeler code 10210

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 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 53 words ▾

Uses • helps prevent sunburn • helps protect against the drying effects of wind • higher SPF gives more sunburn protection • provides moderate protection against 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

⏱️ Dosage and Administration 105 words ▾

Directions • apply generously and evenly 15 minutes before sun exposure and as needed • children under 6 months: Ask a doctor • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours 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 10 a.m. – 2 p.m. • wear long-sleeved shirts, pants, hats and sunglasses Sun Protection Measures:

⚠️ Warnings 53 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. Stop use and ask a doctor if: rash occurs Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 17 words ▾

Active Ingredients Avobenzone (3.0%) Homosalate (10.0%) Octisalate (5.0%) Octocrylene (9.0%) White Petrolatum (31.0%) Purpose Sunscreen Lip Protectant

🧪 Inactive Ingredients 26 words ▾

Inactive Ingredients euphorbia cerifera (candelilla) wax, ozokerite, flavor, paraffin, beeswax, theobroma cacao (cocoa) seed butter, cetyl esters, lanolin, limnanthes alba (meadowfoam) seed oil, stevia rebaudiana extract

🎯 Purpose 4 words ▾

Purpose Sunscreen Lip Protectant

📄 Do Not Use 8 words ▾

Do not use on damaged or broken skin

📄 When Using This Product 13 words ▾

When using this product: keep out of eyes. Rinse with water to remove.

📄 Stop Use and Ask a Doctor If 9 words ▾

Stop use and ask a doctor if: rash occurs

📄 Keep Out of Reach of Children 18 words ▾

Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 6 words ▾

Package Labeling:10210-0056-1 Label11

Package Labeling:10210-0056-2 Label12

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM — the ingredient across all brands.

Top reported reactions

Condition Aggravated2
Drug Dependence1
Illness1
Lip Dry1
Lip Exfoliation1
Lip Pain1
Lip Swelling1

Reporter sex

4 reports
Male · 100%
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 2 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 Carma Laboratories, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 cylinder (10210-0056-01). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Carma Laboratories, Inc. 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.
← 10210-0055-01 · Carma 10210-0057-01 · Carma →
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.