SunDrops 75

Product NDC: 63621-356
Requested package NDC: 63621-356-30
11-digit product format: 636210356
Labeler code: 63621
Product ID: 63621-356_435330fc-c021-151b-e063-6394a90a229b
Type: HUMAN OTC DRUG
Nonproprietary name: Alcohol
Dosage form: GEL
Route: TOPICAL
Labeler: Sunburst Chemicals, Inc.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2009-10-14
Substance: ALCOHOL
Active strength: .6 mL/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	63621-356	63621-356-30	D	Discontinued by firm		2026-08-03

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 · 12 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
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

Additional Listing Data#

Finished product: Yes
Brand name base: SunDrops 75
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	.6 mL/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3K9958V90M	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
581658	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
b0623424-939e-4b49-aa99-c1ef22cf0f2d	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
63621-356-14	SunDrops 75	3785 mL in 1 BOTTLE, PLASTIC	GEL	3785	10
63621-356-20	SunDrops 75	1000 mL in 1 BAG	GEL	1000	10
63621-356-20	SunDrops 75	8 in 1 BOX	GEL	8	10
63621-356-25	SunDrops 75	12 in 1 BOX	GEL	12	10
63621-356-25	SunDrops 75	236.6 mL in 1 BOTTLE, PUMP	GEL	236.6	10
63621-356-30	SunDrops 75	6 in 1 BOX	GEL	6	10
63621-356-30	SunDrops 75	1000 mL in 1 BAG	GEL	1000	10
63621-356-40	SunDrops 75	1000 mL in 1 BAG	GEL	1000	10
63621-356-40	SunDrops 75	4 in 1 BOX	GEL	4	10
63621-356-50	SunDrops 75	473.2 mL in 1 BOTTLE, PUMP	GEL	473.2	10

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
Alcohol	ACTIVE INGREDIENT	3K9958V90M	SUNDROPS 75 (ALCOHOL) GEL [SUNBURST CHEMICALS, INC.]	1
Alcohol	ACTIVE MOIETY	3K9958V90M	SUNDROPS 75 (ALCOHOL) GEL [SUNBURST CHEMICALS, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63621-356	SUNDROPS 75 (ALCOHOL) GEL [SUNBURST CHEMICALS, INC.]	9	Current NDC, Legacy NDC, 10 package rows	20240322_b0623424-939e-4b49-aa99-c1ef22cf0f2d.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SunDrops 75	ALCOHOL	Sunburst Chemicals, Inc.	b0623424-939e-4b49-aa99-c1ef22cf0f2d	2025-11-11	Warnings	Exact identifier ndc (package): 63621-356-30 ndc (product): 63621-356 ndc11 (package): 63621035630

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
581658	ethanol 60 % Topical Gel	PSN	b0623424-939e-4b49-aa99-c1ef22cf0f2d	10
581658	ethanol 0.6 ML/ML Topical Gel	SCD	b0623424-939e-4b49-aa99-c1ef22cf0f2d	10
581658	ethanol 60 % Topical Gel	SY	b0623424-939e-4b49-aa99-c1ef22cf0f2d	10

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63621-356-30	63621035630	6 BAG in 1 BOX (63621-356-30) > 1000 mL in 1 BAG	6 bag	2016-07-20	0000-00-00	No	No	Current