Skip to the page

Data / Drug companies / Randob Labs,ltd. DBA Crossingwell Consumer Health

Randob Labs,ltd. DBA Crossingwell Consumer Health: 17 products in the FDA NDC directory, labeler code 52412

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

Randob Labs,ltd. DBA Crossingwell Consumer Health (labeler code 52412) lists 17 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 17 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on December 30, 2024.

The request: Watch Randob Labs,ltd. DBA Crossingwell Consumer Health (FDA labeler code 52412): 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
52412
Products in commercial distribution
17
Packages
30
Finished drugs by generic name
10
Prescription products
0
Over the counter products
17
Flagged as original packager
17 of 17 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
January 1, 1965
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 drugs1588.2%
Generic drugs (ANDA)211.8%

Products by type

TypeProductsShare
Over the counter drugs17100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Suspension529.4%
Cream423.5%
Liquid211.8%
Solution211.8%
Ointment211.8%
Syrup211.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Single Antibiotic with Bacitracin52412-750OintmentOver the counter monograph drugsDecember 30, 2024
Childrens ibuprofen52412-911SuspensionGeneric drugs (ANDA)July 15, 2023
Fast Acting Pedia Crae52412-912SuspensionOver the counter monograph drugsMay 26, 2023
Pediacare Childrens Cough and Congestion Grape52412-992SyrupOver the counter monograph drugsJanuary 3, 2023
Pediacare Childrens Cough and Cold Grape52412-920SyrupOver the counter monograph drugsJanuary 3, 2023
Pediacare Childrens Ibuprofen Berry52412-910SuspensionGeneric drugs (ANDA)January 3, 2023
Pediacare Childrens Acetaminophen Grape52412-906SuspensionOver the counter monograph drugsJanuary 3, 2023
Pediacare Childrens Grape52412-901SuspensionOver the counter monograph drugsJanuary 3, 2023
Balmex Diaper Rash52412-285CreamOver the counter monograph drugsApril 19, 2021
ERO Ear Wax Removal Kit52412-175LiquidOver the counter monograph drugsApril 16, 2021
Earwax Removal Drops52412-600LiquidOver the counter monograph drugsJuly 3, 2020
Chiggerex52412-350CreamOver the counter monograph drugsFebruary 1, 2020
Fire Out52412-300SolutionOver the counter monograph drugsFebruary 15, 2016
Balmex adult care rash52412-500CreamOver the counter monograph drugsApril 27, 2015
Balmex multi-purpose52412-450OintmentOver the counter monograph drugsApril 27, 2015
Balmex Diaper Rash52412-400CreamOver the counter monograph drugsApril 27, 2015
Sting-Kill52412-200SolutionOver the counter monograph drugsJanuary 1, 1965

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.