Super Lysine Plus Coldstick

Product NDC: 70084-220
11-digit product format: 700840220
Labeler code: 70084
Product ID: 70084-220_419d9734-9a94-c984-e063-6294a90a2dc1
Type: HUMAN OTC DRUG
Nonproprietary name: Octinoxate and Oxybenzone
Dosage form: LIPSTICK
Route: TOPICAL
Labeler: Quantum, Inc.
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1997-01-06
Substance: OCTINOXATE; OXYBENZONE
Active strength: 70; 50 mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 24 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
2025-08-27 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	70084-220-01	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	70084-220-01	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	70084-220-01	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	70084-220-01	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	70084-220-01	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	70084-220-01	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	70084-220-01	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	70084-220-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	70084-220-01	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	70084-220-01	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	70084-220-01	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	70084-220-01	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Super Lysine Plus Coldstick
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	70 mg/g
OXYBENZONE	50 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Y5P7MUD51	Internal UNII lookup
95OOS7VE0Y	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
c9318a8c-ba3b-4068-84df-110c9005ee1d	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
60c52429-fcef-eb54-2387-43bc9e4f296b	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-01-30	Super Lysine + ® Coldstick
2025-01-30	Super Lysine + ® Coldstick
2023-02-13	Super Lysine + ® Coldstick
2023-02-13	Super Lysine + ® Coldstick
2021-01-29	Super Lysine + ® Coldstick
2021-01-29	Super Lysine + ® Coldstick

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70084-220-01	Super Lysine Plus Coldstick	5 g in 1 CYLINDER	LIPSTICK	5		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70084-220	SUPER LYSINE PLUS COLDSTICK (OCTINOXATE AND OXYBENZONE) LIPSTICK [QUANTUM, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20230214_c9318a8c-ba3b-4068-84df-110c9005ee1d.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 32 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Frase Skin SPF 30 Face Sunscreen Activated Vitamin D Technology	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Frase Skin PTY LTD	d904fd23-a3a1-4564-8eec-13a4c96e23f7	2026-05-12	Warnings	Exact identifier application number: M020
Hawaii Sol Natural Non-Nano Sunscreen SPF 50	ZINC OXIDE	Caribbean Sol International, LLC	24678326-547f-427d-a481-d8c40380e30a	2026-05-12	Warnings	Exact identifier application number: M020
Caribbean Sol Natural Non-Nano Sunscreen SPF 50	ZINC OXIDE	Caribbean Sol International, LLC	20aadcf6-16a3-4344-837b-b91ba8753fb0	2026-05-12	Warnings	Exact identifier application number: M020
Cancer Council Daily Face Moisturizer SPF50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Vitality US Co.	1b4333b8-5747-c591-e063-6294a90a9924	2026-05-12	Warnings	Exact identifier application number: M020
Lather Daily Defense Mineral SPF 45 Facial Sunscreen	ZINC OXIDE	Lather, Inc.	50c732a0-b282-d61b-e063-6294a90aa76b	2026-05-12	Warnings	Exact identifier application number: M020
Hampton Sun SPF50 Mineral Face Sunscreen	HOMOSALATE 7.5%, OCTISALATE 5.00%, AVOBENZONE 3.00%	S&C Hampton Sun LLC	f1c5310b-c43b-475d-8a50-d55759ad3164	2026-05-12	Warnings	Exact identifier application number: M020
Even Tone Mineral Sunscreen Broad Spectrum SPF 36 Medium - Dark	TITANIUM DIOXIDE AND ZINC OXIDE	SENT, Inc.	aedde765-931f-430e-9fc3-d87bde2b78cd	2026-05-12	Warnings	Exact identifier application number: M020
Even Tone Mineral Sunscreen Broad Spectrum SPF 40 Light - Medium	TITANIUM DIOXIDE AND ZINC OXIDE	SENT, Inc.	417305d7-d32e-4bc9-8f77-0a42b6bdecf5	2026-05-12	Warnings	Exact identifier application number: M020
Stellar Mineral Glow Guard Sunscreen Broad Spectrum SPF 50	ZINC OXIDE	Stellar Beauty Co.	0f7ee8c6-3af2-42a2-b341-3e0da42c7c93	2026-05-11	Warnings	Exact identifier application number: M020
Frase Skin SPF 50 Activated Vitamin D Technology Cool	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Frase Skin PTY LTD	0a5cc927-0fd3-4c8f-b847-a274f6eb09fb	2026-05-11	Warnings	Exact identifier application number: M020
Miami Beach Bum SPF 30 Bodyguard Face Body Mineral Sunscreen	ZINC OXIDE	Miami Beach Bum	3b778530-9af0-48eb-bd91-d9ac99f2983f	2026-05-11	Warnings	Exact identifier application number: M020
Walgreens SPF 60 Melt-in Milk Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Walgreens	345955ea-f37a-8629-e063-6294a90aa7cc	2026-05-11	Warnings	Exact identifier application number: M020
DERMATONE SPF50 Sunscreen	AVABENZONE 3% HOMOSALATE 10% OCTISALATE 5%	Dermatone Labs LLC	4dc81593-4790-403f-9d49-6569bcd0fea2	2026-05-11	Warnings	Exact identifier application number: M020
The Perfect Derma Mineral Perfection Broad Spectrum SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Bella Medical Products LLC	518f69fc-fd39-8195-e063-6294a90a3fdd	2026-05-11	Warnings	Exact identifier application number: M020
Radical Rescue Morning UVA/UVB Defense Primer Broad Spectrum SPF 30 Universal Tint Mineral Sunscreen	RADICAL RESCUE SPF 30 MINERAL SUNSCREEN	ProTransit, Inc.	38e0139c-bb87-55ba-e063-6294a90a82ee	2026-05-11	Warnings	Exact identifier application number: M020
ChapStick Moisturizer Original SPF 15	SPF 15 SKIN PROTECTANT	Suave Brands Co., LLC	47bfa8ea-4d8d-cd13-e063-6394a90a71aa	2026-05-11	Warnings	Exact identifier application number: M020
EELHOE Sunscreen	TITANIUM DIOXIDE	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	5196ccb0-4515-7e40-e063-6394a90a09bd	2026-05-11	Warnings	Exact identifier application number: M020
Mediheal Madecassoside Moisture Sun Serum	HOMOSALATE, OCTOCRYLENE, OCTISALATE, ENSULIZOLE	74005	47c66535-8287-9b74-e063-6394a90ac3b6	2026-05-10	Warnings	Exact identifier application number: M020
SPF 30 Sunscreen	HOMOSALATE 10% OCTISALATE 5% AVOBENZONE 3%	Coconut Caliente Costa Rica LLC	af56f16a-2643-4bfc-9e05-dfba79cdab8a	2026-05-08	Warnings	Exact identifier application number: M020
Iris and Romeo Weekend Skin Cool Glow	ZINC OXIDE	Iris and Romeo	514f7d70-7b8b-0992-e063-6394a90a1e98	2026-05-08	Warnings	Exact identifier application number: M020

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
70084-220-01	70084022001	5 g in 1 CYLINDER (70084-220-01)	5 g	1997-01-06	No	No	Current