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Data / Drug companies / Jell Pharmaceuticals Pvt. Ltd.

Jell Pharmaceuticals Pvt. Ltd.: 22 products in the FDA NDC directory, labeler code 30400

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Jell Pharmaceuticals Pvt. Ltd. (labeler code 30400) lists 22 products in the FDA National Drug Code Directory, covering 13 finished drugs by generic name. By type: 22 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on February 19, 2025.

The request: Watch Jell Pharmaceuticals Pvt. Ltd. (FDA labeler code 30400): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
30400
Products in commercial distribution
22
Packages
83
Finished drugs by generic name
13
Prescription products
0
Over the counter products
22
Flagged as original packager
14 of 14 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
March 15, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs22100%

Products by type

TypeProductsShare
Over the counter drugs22100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Liquid836.4%
Jelly522.7%
Gel313.6%
Powder29.1%
Ointment29.1%
Granule14.5%
Cream14.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Sunburn Relief Gel30400-605GelOver the counter monograph drugsFebruary 19, 2025
Baby fresh scent petroleum30400-703JellyOver the counter monograph drugsFebruary 15, 2022
Health Smart Vaporizing Chest Rub30400-702GelOver the counter monograph drugsFebruary 15, 2022
Medicated Chest Rub30400-701CreamOver the counter monograph drugsFebruary 14, 2022
Jell with Vitamin A D30400-215OintmentOver the counter monograph drugsJanuary 12, 2022
Shea Butter Petroleum Jelly30400-501JellyOver the counter monograph drugsMay 10, 2021
91% Isopropyl Rubbing Alcohol30400-601LiquidOver the counter monograph drugsJanuary 14, 2021
3 Hydrogen Peroxide30400-250LiquidOver the counter monograph drugsJanuary 10, 2021
Cocoa Butter Petroleum Jelly30400-503JellyOver the counter monograph drugsDecember 24, 2020
Maximum Strength Medicated Foot Powder30400-507PowderOver the counter monograph drugsSeptember 1, 2020
Medicated Body Powder30400-506PowderOver the counter monograph drugsSeptember 1, 2020
91% isopropyl rubbing alcohol with wintergreen30400-707LiquidOver the counter monograph drugsAugust 11, 2020
70% isopropyl rubbing alcohol with wintergreen30400-705LiquidOver the counter monograph drugsAugust 11, 2020
Isopropyl rubbing alcohol 50% with wintergreen30400-101LiquidOver the counter monograph drugsJune 18, 2020
Lavender scent petroleum30400-514JellyOver the counter monograph drugsNovember 1, 2019
Epsom Salts30400-210GranuleOver the counter monograph drugsJuly 9, 2019
Ice Gel ICE COLD ANALGESIC30400-110GelOver the counter monograph drugsApril 2, 2018
Pure Petrolatum Jelly30400-509JellyOver the counter monograph drugsOctober 15, 2016
Isopropyl alcohol 91 percent30400-505LiquidOver the counter monograph drugsMay 30, 2014
Jell Pharmaceuticals Vitamin A D30400-214OintmentOver the counter monograph drugsApril 24, 2014
Isopropyl Rubbing Alcohol30400-100LiquidOver the counter monograph drugsJune 29, 2012
Isopropyl Rubbing Alcohol 70%30400-504LiquidOver the counter monograph drugsMarch 15, 2012

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.