FACE VALUES SPF 15 FACIAL MOISTURIZER

Product NDC: 63940-073
Requested package NDC: 63940-073-05
11-digit product format: 639400073
Labeler code: 63940
Product ID: 63940-073_cee3e430-4905-2772-e053-2a95a90a1dd1
Type: HUMAN OTC DRUG
Nonproprietary name: OCTINOXATE, OCTISALATE, OXYBENZONE
Dosage form: LOTION
Route: TOPICAL
Labeler: HARMON STORES, INC.
Application: part352
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2013-03-08
Marketing end: 0000-00-00
Substance: OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength: 30 mg/mL; mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2022-12-31
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	63940-073	63940-073-05	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	63940-073	63940-073-05	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, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63940-073-05	2021-10-21	C162847	48780-1	c7ccaba7-0f45-fd44-e053-dadaa90aa01b	FACE VALUES OIL-FREE SPF 15 FACIAL MOISTURIZING LOTION
63940-073-05	2021-07-23	C162847	48780-1	c7ccaba7-0f45-fd44-e053-dadaa90aa01b	FACE VALUES OIL-FREE SPF 15 FACIAL MOISTURIZING LOTION

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63940-073	FACE VALUES SPF 15 FACIAL MOISTURIZER (OCTINOXATE, OCTISALATE, OXYBENZONE) LOTION [HARMON STORES, INC.]	4	Legacy NDC	20241023_7afc6766-2262-4f40-b62f-8d39860da113.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
95OOS7VE0Y	OXYBENZONE	131-57-7	OXYBENZONE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
63940-073-05	63940007305	1 BOTTLE, PUMP in 1 CARTON (63940-073-05) > 118 mL in 1 BOTTLE, PUMP (63940-073-04)	2013-03-08	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
FACE VALUES OIL-FREE SPF 15 FACIAL MOISTURIZING LOTION	HARMON STORES, INC.	2024-10-21	HUMAN OTC DRUG LABEL	4