GR CC Broad Spectrum SPF 30

Product NDC: 82715-102
11-digit product format: 827150102
Labeler code: 82715
Product ID: 82715-102_974d4734-afad-4e96-928d-108df2b3774e
Type: HUMAN OTC DRUG
Nonproprietary name: Octinoxate, Oxybenzone
Dosage form: CREAM
Route: TOPICAL
Labeler: ERKUL KOZMETIK SANAYI VE TICARET ANONIM SIRKETI
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-07-22
Marketing end: 2028-05-31
Substance: OCTINOXATE; OXYBENZONE
Active strength: 6; 2 g/100mL; g/100mL
NDC exclude flag: No
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 · 35 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
2025-04-01 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	82715-102-03	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	82715-102-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	82715-102-04	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	82715-102-02	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	82715-102-03	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	82715-102-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	82715-102-04	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	82715-102-02	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	82715-102-03	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	82715-102-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	82715-102-04	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	82715-102-02	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	82715-102-03	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	82715-102-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	82715-102-04	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	82715-102-02	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	82715-102-04	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	82715-102-02	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	82715-102-03	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	82715-102-01	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	82715-102-04	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	82715-102-02	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	82715-102-03	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	82715-102-01	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	82715-102-04	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	82715-102-02	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	82715-102-03	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	82715-102-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: GR CC Broad Spectrum SPF 30

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	6 g/100mL
OXYBENZONE	2 g/100mL

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
751d5194-f5ea-401b-9439-7770510a588c	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75	Product name	2	20250814
cb89b86a-369e-4204-8910-ae797c503af3	Product name	1	20230706
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
d4880ace-a516-8c47-8dfd-73a4ba5887d7	Product name	2	20180830
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
82715-102-01	2025-08-12	GR GOLDEN ROSE CC CREAM COLOR CORRECTING PRIMER
82715-102-02	2025-08-12	GR GOLDEN ROSE CC CREAM COLOR CORRECTING PRIMER
82715-102-03	2025-08-12	GR GOLDEN ROSE CC CREAM COLOR CORRECTING PRIMER
82715-102-04	2025-08-12	GR GOLDEN ROSE CC CREAM COLOR CORRECTING PRIMER
82715-102-01	2025-01-30	GR GOLDEN ROSE CC CREAM COLOR CORRECTING PRIMER
82715-102-02	2025-01-30	GR GOLDEN ROSE CC CREAM COLOR CORRECTING PRIMER
82715-102-03	2025-01-30	GR GOLDEN ROSE CC CREAM COLOR CORRECTING PRIMER
82715-102-04	2025-01-30	GR GOLDEN ROSE CC CREAM COLOR CORRECTING PRIMER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
82715-102-01	GR CC Broad Spectrum SPF 30	30 mL in 1 TUBE	CREAM	30	2
82715-102-01	GR CC Broad Spectrum SPF 30	1 in 1 CARTON	CREAM	1	2
82715-102-02	GR CC Broad Spectrum SPF 30	1 in 1 CARTON	CREAM	1	2
82715-102-02	GR CC Broad Spectrum SPF 30	30 mL in 1 TUBE	CREAM	30	2
82715-102-03	GR CC Broad Spectrum SPF 30	30 mL in 1 TUBE	CREAM	30	2
82715-102-03	GR CC Broad Spectrum SPF 30	1 in 1 CARTON	CREAM	1	2
82715-102-04	GR CC Broad Spectrum SPF 30	30 mL in 1 TUBE	CREAM	30	2
82715-102-04	GR CC Broad Spectrum SPF 30	1 in 1 CARTON	CREAM	1	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82715-102	GR CC BROAD SPECTRUM SPF 30 (OCTINOXATE, OXYBENZONE) CREAM [ERKUL KOZMETIK SANAYI VE TICARET ANONIM SIRKETI]	1	Current NDC, Legacy NDC, 8 package rows	20220803_751d5194-f5ea-401b-9439-7770510a588c.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 86 of 353 · 7,049 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ALOHA MINERAL BLOCK-BRUSH ON MINERAL	SUNSCREEN SPF50	Aopline Biotechnology (Guangzhou) Co., Ltd.	47dd07aa-71b4-5d54-e063-6394a90a4127	2026-01-08	Warnings	Exact identifier application number: M020
SUNSCREEN SETTING SPRITZ, SPF 45	SUNSCREEN SETTING SPRAY	Aopline Biotechnology (Guangzhou) Co., Ltd.	47ddf752-cae2-313f-e063-6294a90a7e3a	2026-01-08	Warnings	Exact identifier application number: M020
St Moriz suncare face sunscreen spf50	OCTOCRYLENE, OCTISALATE , AVOBENZONE , HOMOSALATE	Aopline Biotechnology (Guangzhou) Co., Ltd.	47df072e-151f-eb30-e063-6294a90a4eeb	2026-01-08	Warnings	Exact identifier application number: M020
SUNSCREEN GLOWING	AVOBENZONE ,OCTISALATE ,OCTOCRYLENE , HOMOSALATE	Aopline Biotechnology (Guangzhou) Co., Ltd.	47df0de5-012a-c896-e063-6394a90a9cef	2026-01-08	Warnings	Exact identifier application number: M020
BANANA BOAT	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Edgewell Personal Care Brands LLC	616d35f6-63d2-3d26-e053-2991aa0a5b44	2026-01-08	Warnings	Exact identifier application number: M020
BANANA BOAT	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Edgewell Personal Care Brands LLC	616d35a1-a139-1974-e053-2a91aa0a20b6	2026-01-08	Warnings	Exact identifier application number: M020
PIPA SKIN CARE SUN-SATIONAL Mineral Sunscreen	SPF 30	EVI LABS	258b7b7c-a3f2-172c-e063-6394a90aec6a	2026-01-08	Warnings	Exact identifier application number: M020
DMK Ultrascreen Mineral Sunscreen	ZINC OXIDE	Danne Montague King	3f022275-c1e5-2704-e063-6294a90a4a81	2026-01-08	Warnings	Exact identifier application number: M020
Anhydrous SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Owen Biosciences, Inc.	0cc8221d-5ec5-4abf-a4f5-ab06e8dcea68	2026-01-08	Warnings	Exact identifier application number: M020
Rejuvaskin Mineral Facial Sunscreen SPF 32 Sheer	REJUVASKIN MINERAL FACIAL SUNSCREEN SPF 32 SHEER	Atlantic Medical Products, LLC	47e5198e-7bf6-72a8-e063-6294a90a7ec5	2026-01-08	Warnings	Exact identifier application number: M020
inde wild SUN DEFENSE SPF 50 SUNSCREEN GLOW DROPS BROAD SPECTRUM	INDE WILD SUN DEFENSE GLOW DROPS	INDE WILD PRIVATE LIMITED	47e57407-2925-09ca-e063-6294a90a49ec	2026-01-08	Warnings	Exact identifier application number: M020
NIDA Invisible Fit Sunscreen	SUNSCREEN	Proso Corp	47ed3b62-45ef-b67a-e063-6294a90a317b	2026-01-08	Warnings	Exact identifier application number: M020
Organic Matters SPF 50 Sunscreen	ZINC OXIDE	Veganic SKN Limited	12f37c8d-07f0-3e75-e063-6294a90a2cdf	2026-01-08	Warnings	Exact identifier application number: M020
Ellegreen Sunscreen Broad Spectrum SPF50	ZINC OXIDE	Veganic SKN Limited	161a7209-10d8-928c-e063-6394a90a4139	2026-01-08	Warnings	Exact identifier application number: M020
Live Sunny Eco-zinc hydrating mineral sunscreen for body and face	ZINC OXIDE	Veganic SKN Limited	1a97169e-67be-3d25-e063-6294a90a3b88	2026-01-08	Warnings	Exact identifier application number: M020
Dr Loretta Universal Glow Daily Defense SPF 40	ZINC OXIDE	Dr. Loretta, LLC	1208d0f8-bb12-4574-b70e-3a76b11a64c7	2026-01-07	Warnings	Exact identifier application number: M020
Neutrogena Ultra Sheer Face Sunscreen SPF 60	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	KDC/One Development Corporation, Inc.	259f3fe3-2967-6c05-e063-6394a90a9e45	2026-01-07	Warnings	Exact identifier application number: M020
Hawaiian Blend Extreme Zinc SPF 30	ZINC OXIDE, TITANIUM DIOXIDE	The Islander Group	4084dd98-357f-4011-b0d4-db6536d2931f	2026-01-07	Warnings	Exact identifier application number: M020
Hawaiian Blend Extreme Zinc SPF 50	ZINC OXIDE, TITANIUM DIOXIDE	The Islander Group	9b4acc5e-fdaf-4fcb-83a9-69e430dd43de	2026-01-07	Warnings	Exact identifier application number: M020
Hawaiian Blend Sensitive Zinc SPF 50	ZINC OXIDE, TITANIUM DIOXIDE	The Islander Group	b42261c5-fa6e-4bb3-93c0-97032ab9f716	2026-01-07	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	Marketing end	Sample	Exclude flag	Status
82715-102-01	82715010201	1 TUBE in 1 CARTON (82715-102-01) / 30 mL in 1 TUBE	1 tube	2022-07-22	2028-05-31	No	No	Current
82715-102-02	82715010202	1 TUBE in 1 CARTON (82715-102-02) / 30 mL in 1 TUBE	1 tube	2022-07-22	2028-05-31	No	No	Current
82715-102-03	82715010203	1 TUBE in 1 CARTON (82715-102-03) / 30 mL in 1 TUBE	1 tube	2022-07-22	2028-05-31	No	No	Current
82715-102-04	82715010204	1 TUBE in 1 CARTON (82715-102-04) / 30 mL in 1 TUBE	1 tube	2022-07-22	2028-05-31	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
GR GOLDEN ROSE CC CREAM COLOR CORRECTING PRIMER	ERKUL KOZMETIK SANAYI VE TICARET ANONIM SIRKETI	2025-08-06	HUMAN OTC DRUG LABEL	2