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Salt and Blue Body Sunscreen SPF 30 Zinc Oxide 20% 20 g/100mL Lotion

by Salt + Blue LLC · 1 TUBE in 1 CARTON (87822-845-02) / 86 mL in 1 TUBE
NDC 87822-0845-02
🏷️ FDA NDC (as labeled) 87822-845-02 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

FDA NDC (as labeled) 87822-845-02
Product NDC 87822-845
11-digit billing NDC 87822084502
UNII SOI2LOH54Z
Application # M020
SPL Set ID 47f764a0-e9ad-ef66-e063-6394a90a8de5
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-06-29
Route TOPICAL
Dosage form LOTION
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 87822-845-02 — 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 → 87822-0845-02. 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

LabelerSalt + Blue LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code87822
First marketedJun 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 a topical sunscreen lotion containing 20% zinc oxide, an over-the-counter monograph product marketed under FDA's established rules for sunscreen ingredients. Zinc oxide is a mineral UV filter typically used in sunscreens to help protect skin from ultraviolet radiation. The product is formulated at SPF 30 and comes in a 20 gram lotion base designed for application to the skin.

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 0D145J8EME
    A dried plant extract from aloe ferox, a succulent plant native to South Africa. It's used in medicines as a natural colorant and may help support the product's stability or bitter taste masking.
  • 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 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 2UQQ0PI06P
    A plant-derived oil from lemon myrtle leaves used as a flavoring and fragrance agent in medicines. It provides taste and aroma to make the product more pleasant to take.
  • UNII 39W1PKE3JI
    Bergamot oil is a citrus extract from bergamot orange peel. It's used as a flavoring and fragrance agent to improve taste and aroma in medicines.
  • UNII 9TLV70SV6I
    A natural essential oil extracted from bitter orange peel, used as a flavoring agent to mask unpleasant tastes and improve the palatability of medicines.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII AKN3KSD11B
    Orange oil obtained by cold pressing orange peel. It serves as a flavoring agent and fragrance in medicines to improve taste and aroma.
  • 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 RC25F1T45S
    Elemi oil is a natural resin obtained from elemi trees, used in medicines as a fragrance and flavoring agent to improve taste or aroma of the formulation.
  • UNII TA4JCF9S1J
    A plant oil derived from sea buckthorn berries used as a skin-conditioning agent and emollient in topical formulations to help soften and protect the skin.
  • UNII PAD4FN7P2G
    A fragrant essential oil from juniper wood, used primarily as a flavoring agent and fragrance component to mask tastes and add aroma to medicines.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII 6UYK2W1W1E
    A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
  • UNII 62160PU6FJ
    A natural oil derived from caraway seeds, used as a flavoring agent and solvent to improve taste and help dissolve or mix other ingredients in the medicine.
  • UNII 9S8867952A
    A plant-derived oil from raspberry seeds used as an emollient and skin-conditioning agent in topical formulations. It helps soften the product texture and improve skin feel.
  • 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 MDL271E3GR
    Sorbitan olivate is an emulsifier derived from sorbitol and olive oil. It helps blend water and oil ingredients together to maintain consistent texture and appearance throughout the medicine.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • 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.

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

The official label also states*Helianthus annuus (sunflower) seed oil, sorbitan olivate,* Prunus armeniaca (apricot) kernel oil,* Persea gratissima (avocado) oil,* Olea europaea (Olive) Fruit Oil*, *Rubus idaeus (raspberry) seed oil, *Cera alba (beeswax), *Butyrospermum parkii (shea) butter, *Hippophae rhamnoides (seabuckthorn) fruit oil, *Aloe ferox (aloe) leaf extract, *Caprylic/Capric triglyeride (MCT coconut oil), Pongamia glabra (karanja) seed oil, *Theorbroma cacao (cocoa) seed butter, Tocopherol (non-GMO Vitamin E), Lavandula angustifolia (lavender) oil, *Citrus aurantium bergamia (bergamot) peel oil, *Juniperus virgiana (virginia cedarwood) wood oil, Citrus aurantium amara (bitt orange) leaf/twig oil, Canarium luzonicum (elemi) gum oil, *Citrus aurantium dulcis (orange) peel oil, *Backhousia citriodora (lemon myrtle) leaf oil, *Organically grown or wildcrafted

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
EMMA LEWISHAM Sunceutical SPF 50 Mineral Face Cream 20 g/100mL 84981-0005-01 EMMA 1 jar — — FDA listed —
Hampton Sun SPF 50 Baby Mineral 20 g/100mL 87170-0017-04 S&C 94.6 ml — — FDA listed —
EMMA LEWISHAM Sunceutical SPF 50 Mineral Body Cream 20 g/100mL 84981-0003-01 EMMA 1 jar — — FDA listed —
EMMA LEWISHAM Sunceutical SPF 50 Mineral Glow Serum 20 g/100mL 84981-0002-01 EMMA 1 jar — — FDA listed —
Dermatone Mineral SPF 30 20 g/100mL 54414-0030-02 Dermatone 89 ml — — FDA listed —
Salt and Blue Body Sunscreen SPF 30 20 g/100mLthis 87822-0845-02 Salt 1 tube — — FDA listed —
The Naked Bee SPF 50 Mineral Sunscreen 20 g/100mL 82820-0003-04 The 100 ml — — 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
Jun 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.

🔬 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 Salt and Blue Body Sunscreen SPF 30 (this brand).

Top reported reactions

Sepsis2
Abdominal Abscess1
Abscess1
Blood Magnesium Decreased1
Bradycardia1
Candida Infection1
Candida Test Positive1

Reporter sex

3 reports
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 1 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
87822-0845-02 You're viewing this 1 TUBE in 1 CARTON (87822-845-02) / 86 mL in 1 TUBE 2026-06-29 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 — 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.
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 87822-845-02, 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: 87822-0845-02, written without dashes as 87822084502. 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 87822-0845-02, the first segment (87822) is the labeler code FDA assigned to Salt + Blue LLC; the middle segment (0845) 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 Salt + Blue LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Salt + Blue 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.

📄 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 89 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 risk, regularly use a sunscreen with broad spectrum SPF value of 15 or higher and other sun protection measure including: limit time in the sun, especially from 10 am to 2 pm wear long-sleeved shirts, pants, hats, and sunglasses.

Children under 6 months: ask a doctor.

⏱️ Dosage and Administration 30 words ▾

Uses 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.

⚠️ Warnings 37 words ▾

Warnings For external use only . Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse eyes with water to remove. Stop use and ask a doctor if rash occurs.

🧪 Active Ingredient 5 words ▾

Active Ingredient Zinc Oxide 20%

🧪 Inactive Ingredients 108 words ▾

Inactive Ingredients *Helianthus annuus (sunflower) seed oil, sorbitan olivate,* Prunus armeniaca (apricot) kernel oil,* Persea gratissima (avocado) oil,* Olea europaea (Olive) Fruit Oil*, *Rubus idaeus (raspberry) seed oil, *Cera alba (beeswax), *Butyrospermum parkii (shea) butter, *Hippophae rhamnoides (seabuckthorn) fruit oil, *Aloe ferox (aloe) leaf extract, *Caprylic/Capric triglyeride (MCT coconut oil), Pongamia glabra (karanja) seed oil, *Theorbroma cacao (cocoa) seed butter, Tocopherol (non-GMO Vitamin E), Lavandula angustifolia (lavender) oil, *Citrus aurantium bergamia (bergamot) peel oil, *Juniperus virgiana (virginia cedarwood) wood oil, Citrus aurantium amara (bitt orange) leaf/twig oil, Canarium luzonicum (elemi) gum oil, *Citrus aurantium dulcis (orange) peel oil, *Backhousia citriodora (lemon myrtle) leaf oil, *Organically grown or wildcrafted

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87820-0150-02 · Sundoesmatter 87823-0001-01 · Gummy →
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.