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Data / Drug companies / Buckeye International, Inc.

Buckeye International, Inc.: 15 products in the FDA NDC directory, labeler code 30805

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

Buckeye International, Inc. (labeler code 30805) lists 15 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 15 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on January 1, 2025.

The request: Watch Buckeye International, Inc. (FDA labeler code 30805): 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
30805
Products in commercial distribution
15
Packages
48
Finished drugs by generic name
3
Prescription products
0
Over the counter products
15
Flagged as original packager
15 of 15 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
November 16, 2007
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 drugs15100%

Products by type

TypeProductsShare
Over the counter drugs15100%

Drugs it lists

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

DrugProductsCompanies listing it
Alcohol9293
Benzalkonium chloride4271
Chloroxylenol290

Dosage forms

Dosage formProductsShare
Solution960%
Liquid640%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Altra Foaming Hand Sanitizer Fragrance Free with Aloe and Vitamin E30805-023LiquidOver the counter monograph drugsJanuary 1, 2025
Symmetry Foaming Hand Sanitizer30805-021LiquidOver the counter monograph drugsJanuary 1, 2025
Altra Antimicrobial Foaming Hand Wash w/ Benzalkonium Chloride30805-018SolutionOver the counter monograph drugsNovember 4, 2024
Symmetry Foaming Hand Sanitizer Fragrance Free30805-020LiquidOver the counter monograph drugsJuly 10, 2024
SYMMETRY ANTIMICROBIAL FOAMING HAND WASH w/Benzalkonium Chloride30805-017SolutionOver the counter monograph drugsJune 28, 2022
Altra Antimicrobial Foaming Hand Wash with 0.3% PCMX30805-016SolutionOver the counter monograph drugsApril 15, 2020
Altra Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe30805-015SolutionOver the counter monograph drugsApril 15, 2020
Altra Hand Sanitizer with Aloe and Vitamin E30805-014SolutionOver the counter monograph drugsApril 5, 2020
Altra Foaming Hand Sanitizer Fragrance Free with Aloe and Vitamin E30805-013SolutionOver the counter monograph drugsApril 5, 2020
Altra Foaming Hand Sanitizer with Aloe and Vitamin E30805-012SolutionOver the counter monograph drugsApril 5, 2020
Symmetry Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe30805-010SolutionOver the counter monograph drugsNovember 1, 2011
Symmetry Foaming Hand Sanitizer-Fragrance Free with Aloe and Vitamin E30805-009LiquidOver the counter monograph drugsOctober 4, 2011
Symmetry Antimicrobial Foaming Hand Wash30805-006SolutionOver the counter monograph drugsNovember 16, 2007
Symmetry Foaming Hand Sanitizer30805-003LiquidOver the counter monograph drugsNovember 16, 2007
Symmetry Hand Sanitizer30805-001LiquidOver the counter monograph drugsNovember 16, 2007

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.