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BABY FRESH SCENT PETROLEUM White 99.9 g/100g Jelly, 170 g — NDC 30400-0703-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

BABY FRESH SCENT PETROLEUM White 99.9 g/100g Jelly, 170 g — NDC 30400-703-01 (Billing 30400-0703-01)

by Jell Pharmaceuticals Pvt Ltd. · 170 g in 1 JAR

This is a package of 170 g of BABY FRESH SCENT PETROLEUM White 99.9 g/100g Jelly from Jell Pharmaceuticals Pvt Ltd., marketed since Feb 2022 and currently FDA-listed. It is the main listing for this product, which comes in 4 package sizes.

NDC 30400-0703-01
🏷️ FDA NDC (as labeled) 30400-703-01 billing pads the product segment with a zero
This package
Contains170 g Pack sizes4 compare ↓
Main listing for product 30400-703 · Also comes in: 226 g 30400-703-02 368 g 30400-703-03 510 g 30400-703-04
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) 30400-703-01
Product NDC 30400-703
11-digit billing NDC 30400070301
RxCUI 1302906
UNII 4T6H12BN9U
Application # M016
SPL Set ID d80d21cf-9463-7184-e053-2995a90a23f3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-02-15
Route TOPICAL
Dosage form JELLY
Substance PETROLATUM
Quick answers
  • RxCUI (RxNorm): 1302906
Why two NDCs? The FDA registers this code as 30400-703-01 — 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 → 30400-0703-01. 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?

Baby Fresh Scent Petroleum Jelly is a topical ointment containing petrolatum as its active ingredient. Petrolatum is commonly used as an occlusive moisturizer and skin protectant, helping to seal moisture into the skin and create a barrier against irritants. This product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established safety and use guidelines for this category of skincare products.

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: 226 g 368 g 510 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
30400-0703-01 You're viewing this Main listing 170 g in 1 JAR 2022-02-15 — Active
30400-0703-02 30400-703-02 226 g in 1 JAR 2022-02-15 — Active
30400-0703-03 30400-703-03 368 g in 1 JAR 2022-02-15 — Active
30400-0703-04 30400-703-04 510 g in 1 JAR 2022-02-15 — Active

You're viewing the smallest of 4 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 170 g — 170 g in 1 jar.
How does this package differ from NDC 30400-0703-02?
Both are BABY FRESH SCENT PETROLEUM White 99.9 g/100g Jelly — the drug itself is identical. This page's package is the 170 g one, while NDC 30400-0703-02 is the 226 g package.
What NDC number is used to bill for this package of BABY FRESH SCENT PETROLEUM White 99.9 g/100g Jelly?
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
Baby Fresh Scent Petroleum 99.9 g/100gthis 30400-0703-01 Jell 170 g — — FDA listed —
Novita Petrolatum Jelly Pink 99.9 g/100g 52410-1020-03 Shield 226 g — — FDA listed —
A and D plus E .9985 g/g 64772-0200-03 Derma 368.5 g — — FDA listed —
HealthWise Petroleum Jelly Cocoa Butter 99.89 g/100g 71101-0095-01 Veridian 212 g — — FDA listed —
TheraCare Vitamin A and D plus E 99.85 g/100g 71101-0109-13 Veridian 368 g — — FDA listed —
Universal Baby Fresh Scent Petroleum 99.9 g/100g 52000-0101-01 Universal 170 g — — FDA listed —
Universal Cocoa Butter Scent Petroleum 99.9 g/100g 52000-0102-01 Universal 170 g — — FDA listed —
Universal Lavender Scent Petroleum 99.9 g/100g 52000-0103-01 Universal 170 g — — FDA listed —
Universal Original Petroleum 99.9 g/100g 52000-0104-01 Universal 170 g — — FDA listed —
Health Smart Lavender Baby Petroleum 99.9 g/100g 52862-0011-01 Home 226 g — — FDA listed —
Health Smart Aloe Vera Petroleum 99.9 g/100g 52862-0012-01 Home 226 g — — FDA listed —
Universal Baby Fresh Scent Petroleum 99.9 g/100g 52000-0118-01 Universal 170 g — — FDA listed —
Universal Lavender Scent Petroleum 99.9 g/100g 52000-0150-01 Universal 170 g — — FDA listed —
Health Smart Baby Petroleum 99.9 g/100g 52862-0015-01 Home 226 g — — FDA listed —
Universal Cocoa Butter Scent Petroleum 99.9 g/100g 52000-0119-01 Universal 170 g — — FDA listed —
Health Smart Cocoa Butter Petroleum 99.9 g/100g 52862-0014-01 Home 226 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

🏛️
2022
On the market since
Feb 2022
📍
2026
Currently FDA-listed
4 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 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesInactive ingredients 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.

Manufacturer & labeler

LabelerJell Pharmaceuticals Pvt Ltd.
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code30400
First marketedFeb 2022
Product typeHuman Otc Drug
Portfolio6 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.

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 24 words ▾

Uses For the temporary protection of minor cuts, scrapes, burns and sunburn. Helps to temporarily protect chafed, chapped, cracked or windburned skin and lips.

⏱️ Dosage and Administration 9 words ▾

Directions Apply product as liberally, as often as necessary.

⚠️ Warnings 61 words ▾

Warnings For External Use Only. Do not use over deep or puncture wounds, infections or lacerations. Ask a doctor. When using this product avoid contact with eyes. Stop use and ask doctor if condition worsens or does not improve within 7 days. Keep out of reach of children if swallowed get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 7 words ▾

Active ingredient White Petrolatum USP (99.9 %)

🧪 Inactive Ingredients 3 words ▾

Inactive ingredients Fragrance

🎯 Purpose 3 words ▾

Purpose Skin Protectant

📄 Do Not Use 14 words ▾

Do not use over deep or puncture wounds, infections or lacerations. Ask a doctor.

📄 When Using This Product 8 words ▾

When using this product avoid contact with eyes.

📄 Stop Use and Ask a Doctor If 15 words ▾

Stop use and ask doctor if condition worsens or does not improve within 7 days.

📄 Keep Out of Reach of Children 19 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 1 words ▾

Label

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 BABY FRESH SCENT PETROLEUM (this brand).

Top reported reactions

Pyrexia8
Pneumonia7
Palmar-plantar Erythrodysaesthesia Syndrome6
Renal Failure6
Hypertension5
Blood Creatinine Increased4
Decreased Appetite4

Age at onset

Adult5
Elderly6

Reporter sex

0 reports

Serious outcomes

Death19
Life-threatening15
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 4 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 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 226 g (30400-0703-02), 368 g (30400-0703-03), 510 g (30400-0703-04). 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.
← 30400-0702-01 · Jell 30400-0705-01 · 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.