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Data / Drug companies / Home Smart Products

Home Smart Products: 20 products in the FDA NDC directory, labeler code 52862

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

Home Smart Products (labeler code 52862) lists 20 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 20 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on November 1, 2026.

The request: Watch Home Smart Products (FDA labeler code 52862): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
52862
Products in commercial distribution
20
Packages
101
Finished drugs by generic name
8
Prescription products
0
Over the counter products
20
Flagged as original packager
20 of 20 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
July 28, 2013
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 drugs20100%

Products by type

TypeProductsShare
Over the counter drugs20100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Jelly735%
Liquid630%
Gel315%
Granule210%
Powder15%
Cloth15%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Wet Wipes Antibacterial Travel Pack52862-656ClothOver the counter monograph drugsNovember 1, 2026
Blue Ice Topical Analgesic Gel52862-901GelOver the counter monograph drugsJanuary 1, 2024
White rain Cocoa Butter Petroleum Jelly52862-133JellyOver the counter monograph drugsJanuary 8, 2022
White Rain Original Petroleum52862-131JellyOver the counter monograph drugsJanuary 8, 2022
91% Isopropyl Rubbing Alcohol52862-028LiquidOver the counter monograph drugsJanuary 14, 2021
Isopropyl rubbing alcohol 99% with wintergreen52862-029LiquidOver the counter monograph drugsJune 18, 2020
Isopropyl rubbing alcohol 70% with wintergreen52862-025LiquidOver the counter monograph drugsJune 18, 2020
Isopropyl Rubbing Alcohol 70%52862-024LiquidOver the counter monograph drugsJune 18, 2020
Isopropyl rubbing alcohol 50% with wintergreen52862-023LiquidOver the counter monograph drugsJune 18, 2020
Isopropyl Rubbing Alcohol 50%52862-022LiquidOver the counter monograph drugsJune 18, 2020
Epsom Salts52862-203GranuleOver the counter monograph drugsJuly 9, 2019
Epsom Salts52862-202GranuleOver the counter monograph drugsJuly 9, 2019
Health Smart Medicated Body52862-030PowderOver the counter monograph drugsFebruary 27, 2014
Health Smart Vaporizing Chest Rub52862-902GelOver the counter monograph drugsOctober 1, 2013
Health Smart Vaporizing Chest Rub52862-041GelOver the counter monograph drugsOctober 1, 2013
Health Smart Baby Petroleum52862-015JellyOver the counter monograph drugsJuly 28, 2013
Health Smart Cocoa Butter Petroleum52862-014JellyOver the counter monograph drugsJuly 28, 2013
Health Smart Original Petroleum52862-013JellyOver the counter monograph drugsJuly 28, 2013
Health Smart Aloe Vera Petroleum52862-012JellyOver the counter monograph drugsJuly 28, 2013
Health Smart Lavender Baby Petroleum52862-011JellyOver the counter monograph drugsJuly 28, 2013

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.