Saccharum officinale

Product NDC: 71919-601
Requested package NDC: 71919-601-08
11-digit product format: 719190601
Labeler code: 71919
Product ID: 71919-601_c2504498-d090-4e27-a5ed-e7db6f90abe4
Type: HUMAN OTC DRUG
Nonproprietary name: SUCROSE
Dosage form: LIQUID
Route: ORAL
Labeler: Washington Homeopathic Products
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2010-11-16
Marketing end: 0000-00-00
Substance: SUCROSE
Active strength: 30 [hp_C]/mL
NDC exclude flag: No
Listing certified through: 2020-12-31
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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	71919-601	71919-601-08	I	Inactivated by FDA		2026-08-07

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 · 9 matching rows.

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

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
71919-601-07	DRUG FACTS
71919-601-08	DRUG FACTS
71919-601-09	DRUG FACTS
71919-601-10	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71919-601-07	Saccharum officinale	15 mL in 1 VIAL, GLASS	LIQUID	15	1
71919-601-08	Saccharum officinale	30 mL in 1 VIAL, GLASS	LIQUID	30	1
71919-601-09	Saccharum officinale	50 mL in 1 BOTTLE, GLASS	LIQUID	50	1
71919-601-10	Saccharum officinale	100 mL in 1 BOTTLE, GLASS	LIQUID	100	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71919-601	SACCHARUM OFFICINALE (SUCROSE) LIQUID [WASHINGTON HOMEOPATHIC PRODUCTS]	1	Legacy NDC, 4 package rows	20180126_e3c10dfb-9b0c-49fa-84d4-8421c3c4410f.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
C151H8M554	SUCROSE	57-50-1	SUCROSE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71919-601-08	71919060108	30 mL in 1 VIAL, GLASS (71919-601-08)	30 ml	2010-11-16	0000-00-00	No	No	Current