FACE VALUES ULTRA SPORT ACTIVE SPF 30 SUNSCREEN

Product NDC: 63940-067
Requested package NDC: 63940-067-11
11-digit product format: 639400067
Labeler code: 63940
Product ID: 63940-067_f119e412-c34c-7b9a-e053-2a95a90ac57b
Type: HUMAN OTC DRUG
Nonproprietary name: AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form: LOTION
Route: TOPICAL
Labeler: HARMON STORES, INC.
Application: part352
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2008-02-29
Marketing end: 0000-00-00
Substance: AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength: 30 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2023-12-31
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	63940-067	63940-067-11	D	Discontinued by firm		2026-10-05

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 · 1 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	63940-067	63940-067-11	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
63940-067-09	2021-10-21	FACE VALUES ULTRA SPORT ACTIVE SPF 30 SUNSCREEN LOTION
63940-067-11	2021-10-21	FACE VALUES ULTRA SPORT ACTIVE SPF 30 SUNSCREEN LOTION
63940-067-09	2021-07-23	FACE VALUES ULTRA SPORT ACTIVE SPF 30 SUNSCREEN LOTION
63940-067-11	2021-07-23	FACE VALUES ULTRA SPORT ACTIVE SPF 30 SUNSCREEN LOTION

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63940-067	FACE VALUES ULTRA SPORT ACTIVE SPF 30 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [HARMON STORES, INC.]	5	Legacy NDC	20241023_48dd695d-08b3-43f6-8694-1999c33710fb.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63940-067-11	63940006711	237 mL in 1 PACKAGE (63940-067-11)	237 ml	2008-02-29	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
FACE VALUES ULTRA SPORT ACTIVE SPF 30 SUNSCREEN LOTION	HARMON STORES, INC.	2024-10-21	HUMAN OTC DRUG LABEL	5