Epigenetic Support Formula

Product NDC
73512-0001
Requested package NDC
73512-0001-1
11-digit product format
735120001
Labeler code
73512
Product ID
73512-0001_bc9e3e63-98ee-4842-97c2-2f0e4ebdbf96
Type
HUMAN OTC DRUG
Nonproprietary name
Natrum Muriaticum, Magnesia Phosphorica
Dosage form
LIQUID
Route
ORAL
Labeler
Rainey Chiropractic, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-03-27
Marketing end
0000-00-00
Substance
SODIUM CHLORIDE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Active strength
3 [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage73512-000173512-0001-1DDiscontinued by firm2026-10-20

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage73512-000173512-0001-1DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage73512-000173512-0001-1DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73512-0001-17351200010160 mL in 1 BOTTLE, DROPPER (73512-0001-1) 60 ml2020-03-270000-00-00NoNoCurrent