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Shea Butter Petroleum Jelly Petrolatum 99.6 g/100g Jelly, 283 g — NDC 30400-0501-08 package photo

Shea Butter Petroleum Jelly Petrolatum 99.6 g/100g Jelly, 283 g

by Jell Pharmaceuticals Pvt. Ltd. · 283 g in 1 JAR (30400-501-08)
NDC 30400-0501-08
🏷️ FDA NDC (as labeled) 30400-501-08 billing pads the product segment with a zero
This package
Contains283 g Pack sizes8 compare ↓
Also comes in: 49 g 30400-0501-02 100 g 30400-0501-03 113 g 30400-0501-04 170 g 30400-0501-05 226 g 30400-0501-07 368 g 30400-0501-01 425 g 30400-0501-06
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) 30400-501-08
Product NDC 30400-501
11-digit billing NDC 30400050108
RxCUI 1252009
UNII 4T6H12BN9U
Application # M016
SPL Set ID cd848f33-e863-d3af-e053-2a95a90a45b1
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-05-10
Route TOPICAL
Dosage form JELLY
Substance PETROLATUM
Why two NDCs? The FDA registers this code as 30400-501-08 — 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 → 30400-0501-08. 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

LabelerJell Pharmaceuticals Pvt. Ltd.
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code30400
First marketedMay 2021
Product typeHuman Otc Drug
Portfolio11 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?

This is an over-the-counter topical jelly containing petrolatum, marketed under FDA's OTC monograph rules for skin protectants. Petrolatum is a mineral oil-based ingredient typically used to help protect and soften skin and to lock in moisture on areas of dryness or minor irritation. The product is applied directly to the skin surface and is commonly used for chapped lips, minor cuts, and general skin conditioning.

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.

💊 What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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.

  • 0.1 g / 100 g 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.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesbutyrospermum parkii (shea butter), fragrance

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 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: 49 g 100 g 113 g 170 g 226 g 368 g 425 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Shea Butter Petroleum Jelly 99.6 g/100g 00363-0740-13 Walgreens 368 g — — FDA listed —
Shea Butter Petroleum Jelly 99.6 g/100gthis 30400-0501-08 Jell 283 g — — FDA listed —
Baby Petrolatum Jelly 99.9 g/100g 52410-0206-02 SHIELD 226 g — — FDA listed —
Petroleum Jelly Cocoa Butter Scent 3.53oz 99.6 g/100g 57337-0163-01 Rejoice 100 g — — FDA listed —
Petrolatum Jelly 99.6 g/100g 77338-0162-01 ASTONEA 100 g — — 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

🏛️
2021
On the market since
May 2021
📍
2026
Currently FDA-listed
5 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
30400-0501-01 368 g in 1 JAR (30400-501-01) 2021-10-11 Active
30400-0501-02 49 g in 1 JAR (30400-501-02) 2021-10-11 Active
30400-0501-03 100 g in 1 JAR (30400-501-03) 2021-10-11 Active
30400-0501-04 113 g in 1 JAR (30400-501-04) 2021-10-11 Active
30400-0501-05 170 g in 1 JAR (30400-501-05) 2021-10-11 Active
30400-0501-06 425 g in 1 JAR (30400-501-06) 2021-10-11 Active
30400-0501-07 226 g in 1 JAR (30400-501-07) 2021-10-11 Active
30400-0501-08 You're viewing this 283 g in 1 JAR (30400-501-08) 2021-10-11 Active

You're viewing one of 8 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 30400-0501-08?
NDC 30400-0501-08 contains 283 g — 283 g in 1 jar.
What is the difference between NDC 30400-0501-08 and NDC 30400-0501-02?
Both are Shea Butter Petroleum Jelly Petrolatum 99.6 g/100g Jelly — the drug itself is identical. NDC 30400-0501-08 is the 283 g package, while NDC 30400-0501-02 is the 49 g package.
What NDC number is used to bill for this package of Shea Butter Petroleum Jelly Petrolatum 99.6 g/100g Jelly?
Bill NDC 30400-0501-08 — the 11-digit billing format is 30400050108. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 30400-501-08, 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: 30400-0501-08, written without dashes as 30400050108. 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 30400-0501-08, the first segment (30400) is the labeler code FDA assigned to Jell Pharmaceuticals Pvt. Ltd.; the middle segment (0501) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (08) 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 Jell Pharmaceuticals Pvt. Ltd.. 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 7 other package presentations of this same product, including 49 g (30400-0501-02), 100 g (30400-0501-03), 113 g (30400-0501-04). 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?
Jell Pharmaceuticals Pvt. 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.

📄 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 ▾

When using this product do not get into eyes

⏱️ Dosage and Administration 4 words ▾

Directions apply as needed

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 6 words ▾

Active Ingredient White Petrolatum USP (99.6%)

🧪 Inactive Ingredients 7 words ▾

Inactive ingredients butyrospermum parkii (shea butter), fragrance

🎯 Purpose 3 words ▾

Purpose Skin Protectant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 30400-0250-01 · Jell 30400-0503-01 · Jell →
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.