DNA

Product NDC: 52654-0002
Requested package NDC: 52654-0002-1
11-digit product format: 526540002
Labeler code: 52654
Product ID: 52654-0002_1417c053-f874-45ed-bdd8-63297e4872d7
Type: HUMAN OTC DRUG
Nonproprietary name: DNA
Dosage form: LIQUID
Route: ORAL
Labeler: Chi Research Inc
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2012-10-09
Substance: HERRING SPERM DNA
Active strength: 12 [hp_X]/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	52654-0002	52654-0002-1	D	Discontinued by firm		2026-09-14

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 · 8 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	`8dfbde2a14a4…`	`c9ff85d89658…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2024-07-12	DRUG FACTS:
2024-07-12	DRUG FACTS:
2021-01-29	DRUG FACTS:
2021-01-29	DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52654-0002-1	DNA	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
HERRING SPERM DNA	ACTIVE INGREDIENT	51FI676N6F	DNA LIQUID [CHI RESEARCH INC]	1
HERRING SPERM DNA	ACTIVE MOIETY	51FI676N6F	DNA LIQUID [CHI RESEARCH INC]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	DNA LIQUID [CHI RESEARCH INC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	DNA LIQUID [CHI RESEARCH INC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52654-0002	DNA LIQUID [CHI RESEARCH INC]	3	Current NDC, Legacy NDC, 1 package rows	20240713_14300ff6-03c7-4f0b-ad95-76761f89a6ff.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
51FI676N6F	HERRING SPERM DNA	HERRING SPERM DNA

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
52654-0002-1	52654000201	60 mL in 1 BOTTLE, DROPPER (52654-0002-1)	60 ml	2019-08-09	No	No	Historical

DNA