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Jell Pharmaceuticals Vitamin A D Petrolatum .76 g/g Ointment, 425.25 g — NDC 30400-214-02 (Billing 30400-0214-02)

by Jell Pharmaceuticals Pvt. Ltd. · 425.25 g in 1 JAR

This is a package of 425.25 g of Jell Pharmaceuticals Vitamin A D Petrolatum .76 g/g Ointment from Jell Pharmaceuticals Pvt. Ltd., marketed since Apr 2014 and currently FDA-listed.

NDC 30400-0214-02
🏷️ FDA NDC (as labeled) 30400-214-02 billing pads the product segment with a zero
This package
Contains425.25 g Pack sizes4 compare ↓
Product page 30400-0214-01 Also comes in: 28.35 g 30400-214-03 56.7 g 30400-214-04 113.4 g 30400-214-01
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 30400-214-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
30400 labeler · 214 product · 02 package
Package marketed since
Jul 1, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0616784115511
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 30400-214-02
Product NDC 30400-214
11-digit billing NDC 30400021402
RxCUI 1049072
UNII 4T6H12BN9U
UPC 0616784115511
Application # M016
SPL Set ID 6ab8ba54-3679-4fd0-a876-cb89aace96ca
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-04-24
Route TOPICAL
Dosage form OINTMENT
Substance PETROLATUM
Quick answers
  • RxCUI (RxNorm): 1049072
Why two NDCs? The FDA registers this code as 30400-214-02 — 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 → 30400-0214-02. 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 topical ointment containing petrolatum as its active ingredient. Petrolatum is a mineral oil-based occlusive agent typically used on skin to help retain moisture and protect against irritation. The product is marketed under FDA's OTC monograph rules for skin protectant ointments. It is applied directly to the skin surface and is commonly found in products intended to soothe and moisturize dry or irritated areas.

Supplement & herbal interactions

Some supplements/herbs that may interact with Petrolatum — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Petrolatum (3 interactions) — ranked by severity →
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 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.
Try another pack size: 28.35 g 56.7 g 113.4 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
30400-0214-01 30400-214-01 Main listing 113.4 g in 1 TUBE 2020-07-01 — Active
30400-0214-02 You're viewing this 425.25 g in 1 JAR 2020-07-01 — Active
30400-0214-03 30400-214-03 28.35 g in 1 TUBE 2020-07-01 — Active
30400-0214-04 30400-214-04 56.7 g in 1 TUBE 2020-07-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 425.25 g — 425.25 g in 1 jar.
How does this package differ from NDC 30400-0214-03?
Both are Jell Pharmaceuticals Vitamin A D Petrolatum .76 g/g Ointment — the drug itself is identical. This page's package is the 425.25 g one, while NDC 30400-0214-03 is the 28.35 g package.
What NDC number is used to bill for this package of Jell Pharmaceuticals Vitamin A D Petrolatum .76 g/g Ointment?
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
Jell Pharmaceuticals Vitamin A D .76 g/gthis 30400-0214-02 Jell 425.25 g — — FDA listed —
health beyond VITAMINS AD 76 g/100g 43473-0091-01 Nantong 5 g — — FDA listed —
MedPride Vitamin A and D 76 g/100g 52410-3045-02 Shield 5 g — — FDA listed —
Vitamin A and D 76 g/100g 57896-0110-14 Geri-care 144 packets — — FDA listed —
A and D 76 g/100g 61010-4405-01 Safetec 113.4 g — — FDA listed —
Vitamin A D .76 g/g 67777-0214-03 Dynarex 12 jars — — FDA listed —
DABUR Vitamin A and D 76 g/100g 68747-3045-02 Dabur 5 g — — FDA listed —
Vitamin A and D 76 g/100g 69396-0121-05 Trifecta 144 packets — — FDA listed —
Astonea Vitamin A and D 76 g/100g 77338-0307-02 ASTONEA 5 g — — FDA listed —
Hammertech Vitamin A and D 76 g/100g 83499-0001-02 HAMMER 5 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

🏛️
2014
On the market since
Apr 2014
📍
2026
Currently FDA-listed
12 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerJell Pharmaceuticals Pvt. Ltd.
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code30400
First marketedApr 2014
Product typeHuman Otc Drug
Portfolio11 products on file

More NDCs from Jell Pharmaceuticals Pvt. Ltd. labeler code 30400

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 24 words ▾

Indications & Usage Directions for diaper rash: Change wet and soiled diapers promptly Cleanse the diaper area and allow to dry Apply as needed

⏱️ Dosage and Administration 29 words ▾

Dosage & Administration Stop use and ask a doctor if: If condition worsens symptoms last more than 7 days or clear up and occur again in a few days

⚠️ Warnings 5 words ▾

Warnings: For External Use Only

🧪 Active Ingredient 9 words ▾

Active Ingredient Purpose White Petrolatum USP (76%) Skin Protectant

🧪 Inactive Ingredients 11 words ▾

Inactive Ingredients: Inactive Ingredients: Light Liquid Parafin, Vitamin A, Vitamin D

🎯 Purpose 74 words ▾

Purpose: Helps treat and prevent diaper rash Helps seal out wetness Temporarily protects minor * cuts * scrapes * burns Temporarily helps protect and help relieve chapped and cracked skin and lips Helps prevent and protect from the drying effects of wind and cold weather Helps prevent and protect chafed skin or minor skin irritations associated with diaper rash With each diaper change, especially at bedtime when exposure to wet diapers may be prolonged

📄 Do Not Use 14 words ▾

Do not use: Do not use: Deep or puncture wounds animal bites serious burns

📄 When Using This Product 9 words ▾

When using this product: Do not get in eyes

📄 Keep Out of Reach of Children 25 words ▾

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

📄 Package Label / Principal Display Panel 9 words ▾

Principal Display Panel Jell Vit AD.jpg Jell Vit AD

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 Jell Pharmaceuticals Vitamin A D (this brand).

Top reported reactions

Rash45
Pneumonia31
Pruritus31
Cellulitis29
Dyspnoea24
Urinary Tract Infection24
Dizziness23

Age at onset

Neonate5
Infant3
Child9
Adolescent3
Adult57
Elderly59

Reporter sex

435 reports

Serious outcomes

Hospitalization260
Death72
Life-threatening49
Disabling8
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 71 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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 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 3 other package presentations of this same product, including 28.35 g (30400-0214-03), 56.7 g (30400-0214-04), 113.4 g (30400-0214-01). 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?
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.
← 30400-0210-01 · Jell 30400-0215-10 · 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.