Cold Plasma Plus Neck and Chest SPF25

Product NDC: 45634-167
11-digit product format: 456340167
Labeler code: 45634
Product ID: 45634-167_dbd71b03-b2f6-2a75-e053-2a95a90ad3eb
Type: HUMAN OTC DRUG
Nonproprietary name: titanium dioxide
Dosage form: CREAM
Route: TOPICAL
Labeler: NV Perricone LLC
Application: M020
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2022-04-01
Marketing end: 0000-00-00
Substance: TITANIUM DIOXIDE
Active strength: 1 g/30g
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	45634-167		I	Inactivated by FDA		2026-10-05
excluded package	package	45634-167	45634-167-31	I	Inactivated by FDA		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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	45634-167-31	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	45634-167-31	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	45634-167-31	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	45634-167-31	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	45634-167-31	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	45634-167-31	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	45634-167-31	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	45634-167-31	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	45634-167-31	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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
45634-167-31	2025-01-30	C162847	48780-1	2cef2736-aa5e-d83d-e063-dadaa90ab31f	db954edf-f530-3bbd-e053-2995a90a8ebe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
45634-167-31	Cold Plasma Plus Neck and Chest SPF25	8 g in 1 BOTTLE, GLASS	CREAM	8		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
45634-167	COLD PLASMA PLUS NECK AND CHEST SPF25 (TITANIUM DIOXIDE) CREAM [NV PERRICONE LLC]	4	Legacy NDC, 1 package rows	20230906_db954edf-f530-3bbd-e053-2995a90a8ebe.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 30 of 361 · 7,213 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Freaks of Nature Peak Performance Broad Spectrum SPF 50	FREAKS OF NATURE PEAK PERFORMANCE BROAD SPECTRUM SPF 50	THE FREAKS OF NATURE, INC.	5247187d-a14c-6468-e063-6394a90ace3e	2026-05-20	Warnings	Exact identifier application number: M020
Journee Bio-restorative Day Balm Broad-spectrum Suncreen SPF 30	OCTINOXATE AND ZINC OXIDE	Merz North America, Inc.	e120a659-0dfc-42ca-8158-58e8a0b457e5	2026-05-20	Warnings	Exact identifier application number: M020
Evereden Cooling Mineral Sunstick SPF 30	ZINC OXIDE	Eden Brands Inc.	4af9e668-0d88-74ad-e063-6394a90a5243	2026-05-19	Warnings	Exact identifier application number: M020
Freaks of Nature Peak Performance Broad Spectrum SPF 30	FREAKS OF NATURE PEAK PERFORMANCE BROAD SPECTRUM SPF 30	THE FREAKS OF NATURE, INC.	522addd5-9701-3234-e063-6294a90aaa9d	2026-05-19	Warnings	Exact identifier application number: M020
Freaks of Nature Peak Performance Broad Spectrum SPF 30	FREAKS OF NATURE PEAK PERFORMANCE BROAD SPECTRUM SPF 30	THE FREAKS OF NATURE, INC.	522b4aca-fe5b-dfe2-e063-6394a90ae578	2026-05-19	Warnings	Exact identifier application number: M020
SP-FFC3-L0TN Barrier Protection Hydrating Mineral Face Sunscreen	BARRIER PROTECTION HYDRATING MINERAL FACE SUNSCREEN	Epic Etailers, LLC (DBA: Beauty by Earth)	5078479e-a196-7e4d-e063-6394a90ab266	2026-05-19	Warnings	Exact identifier application number: M020
InvisibleMatteBarrierDefenseCeramideSunscreenSerumSPF30SP-FSRM-N0TT	INVISIBLE MATTE BARRIER DEFENSE CERAMIDE SUNSCREEN SERUM SPF 30	Epic Etailers, LLC (DBA: Beauty by Earth)	50790945-f359-07c8-e063-6294a90a5af9	2026-05-19	Warnings	Exact identifier application number: M020
Sun Bum Amazon 8 OZ SPF 15	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum	522fc8a4-ce9f-8be8-e063-6294a90aebf0	2026-05-19	Warnings	Exact identifier application number: M020
Timesavvy Hybrid Sheer Sun Serum Broad Spectrum SPF 50	HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE	PROBETTER USA INC.	66624df4-cb6c-4cfb-bbbe-9f885f2ad778	2026-05-18	Warnings	Exact identifier application number: M020
Hampton Sun SPF 50	AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 %	S&C Hampton Sun LLC	4df050f9-1185-4ee4-a0cd-84ba9d254e58	2026-05-18		Exact identifier application number: M020
Hampton Sun SPF 70 Kids	AVOBENZONE, HUMOSALATE, OCTISALATE, OCTOCRYLENE	S&C Hampton Sun LLC	7c976082-3265-4c0b-9985-277d27988895	2026-05-18	Warnings	Exact identifier application number: M020
Evereden Kids Cooling Mineral Sunstick SPF30	ZINC OXIDE	Eden Brands Inc.	521afa81-737f-81d4-e063-6394a90ad307	2026-05-18	Warnings	Exact identifier application number: M020
cle de peau BEAUTE RESTORATIVE DAY SUPREME	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Shiseido Americas Corporation	157e52c5-f6fa-430b-bbb8-86b7c0868ad3	2026-05-18	Warnings	Exact identifier application number: M020
cle de peau BEAUTE SKIN BEAUTY ENHANCER	AVOBENZONE, OCTISALATE, AND OCTOCRYLENE	Shiseido Americas Corporation	bc6230f1-dba2-4418-b48c-c5e67aebd1bd	2026-05-18	Warnings	Exact identifier application number: M020
Hampton Sun SPF 30 SILK BODY	AVOBENZONE, HUMOSALATE, OCTISALATE, OCTOCRYLENE	S&C Hampton Sun LLC	ed0c184d-473a-4c4c-b6ec-e1d79ad58460	2026-05-18	Warnings	Exact identifier application number: M020
Sheer Defense Tinted SPF 46	ZINC OXIDE, OCTINOXATE	Private Label Skin Care	017265e9-31e6-43ce-9432-cb88f471c496	2026-05-18	Warnings	Exact identifier application number: M020
Aveeno Daily Moisturizing Face Sunscreen Broad Spectrum SPF30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Kenvue Brands LLC	51d59378-df72-e438-e063-6294a90a97f1	2026-05-15	Warnings	Exact identifier application number: M020
Natural Sense SPF 50 Sunscreen	SUNSCREEN	Dr. Natural LLC	49a2430e-c15b-4610-e063-6294a90ac520	2026-05-15	Warnings	Exact identifier application number: M020
LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM	TITANIUM DIOXIDE AND ZINC OXIDE	LOreal USA Products Inc.	23cc5ff4-f842-4e3e-ac5c-23dbaf7d3914	2026-05-15	Warnings	Exact identifier application number: M020
LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM	TITANIUM DIOXIDE AND ZINC OXIDE	SICOS ET CIE	c688f8e6-2cd2-40db-b03f-90fd74c2d89c	2026-05-15	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
45634-167-31	45634016731	8 g in 1 BOTTLE, GLASS (45634-167-31)	8 g	2022-04-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Cold Plasma Plus Neck and Chest SPF25 - NV Perricone LLC	NV Perricone LLC	2023-09-05	HUMAN OTC DRUG LABEL	4