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Data / Drug companies / White Manufacturing Inc. DBA Micro-West

White Manufacturing Inc. DBA Micro-West: 18 products in the FDA NDC directory, labeler code 61657

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

White Manufacturing Inc. DBA Micro-West (labeler code 61657) lists 18 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 16 over the counter drugs, 2 prescription drugs. Its main marketing category is unapproved homeopathic products. The newest product started marketing on November 1, 2018.

The request: Watch White Manufacturing Inc. DBA Micro-West (FDA labeler code 61657): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
61657
Products in commercial distribution
18
Packages
18
Finished drugs by generic name
2
Prescription products
2
Over the counter products
16
Flagged as original packager
18 of 18 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
August 1, 1993
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Unapproved homeopathic products18100%

Products by type

TypeProductsShare
Over the counter drugs1688.9%
Prescription drugs211.1%

Drugs it lists

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

DrugProductsCompanies listing it
Aluminum metal11
Mercurius vivus12

Dosage forms

Dosage formProductsShare
Liquid18100%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Total fem bal61657-2971LiquidUnapproved homeopathic productsNovember 1, 2018
Total andro bal61657-2970LiquidUnapproved homeopathic productsNovember 1, 2018
Total tri-estro61657-2969LiquidUnapproved homeopathic productsNovember 1, 2018
Total flu cld 161657-2968LiquidUnapproved homeopathic productsNovember 1, 2018
Hpz61657-2327LiquidUnapproved homeopathic productsNovember 1, 2018
Chron sino61657-2104LiquidUnapproved homeopathic productsNovember 1, 2018
Total Aluminum61657-0955LiquidUnapproved homeopathic productsSeptember 30, 2011
Total pro-jes61657-0974LiquidUnapproved homeopathic productsSeptember 15, 2011
Allerhale61657-0003LiquidUnapproved homeopathic productsSeptember 1, 2011
Surgery/Trauma61657-0904LiquidUnapproved homeopathic productsJuly 1, 2011
Bactoflam61657-0052LiquidUnapproved homeopathic productsJune 10, 2011
Anxiolix61657-0006LiquidUnapproved homeopathic productsJune 1, 2011
Total mercury61657-0961LiquidUnapproved homeopathic productsJanuary 1, 2011
Met-Tox61657-0526LiquidUnapproved homeopathic productsJanuary 24, 2006
Whole System EEP61657-0208LiquidUnapproved homeopathic productsMay 21, 2005
Thyroid61657-0952LiquidUnapproved homeopathic productsAugust 26, 1996
Vermafuge -AG Lycopodium61657-1026LiquidUnapproved homeopathic productsAugust 3, 1993
Cand-ex61657-0101LiquidUnapproved homeopathic productsAugust 1, 1993

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.