CONTROL CORRECTIVE TINTED MOISTURIZER

Product NDC: 70764-206
11-digit product format: 707640206
Labeler code: 70764
Product ID: 70764-206_474c088c-d530-c933-e063-6294a90a21ae
Type: HUMAN OTC DRUG
Nonproprietary name: TITANIUM DIOXIDE, ZINC OXIDE
Dosage form: CREAM
Route: TOPICAL
Labeler: CONTROL CORRECTIVE SKINCARE INC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-09-11
Substance: TITANIUM DIOXIDE; ZINC OXIDE
Active strength: 2.5; 6 g/100mL; g/100mL
Pharmacologic classes: Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 · 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	70764-206-52	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	70764-206-52	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	70764-206-52	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	70764-206-52	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	70764-206-52	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	70764-206-52	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	70764-206-52	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	70764-206-52	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	70764-206-52	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: CONTROL CORRECTIVE TINTED MOISTURIZER
Brand name suffix: SPF-30 SUNSCREEN
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TITANIUM DIOXIDE	2.5 g/100mL
ZINC OXIDE	6 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
15FIX9V2JP	Internal UNII lookup
SOI2LOH54Z	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
8ac09149-f7e7-40a8-b306-98964d0cd6e3	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f47a510b-6679-4664-b2d6-47b5c4afe7cc	Product name	4	20260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
190f2a5b-bbc8-65c7-fcb0-97891307b917	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70764-206-52	2025-12-31	C162847	48780-1	2cef2736-62a0-d83d-e063-dadaa90ab31f	CONTROL CORRECTIVE TINTED MOISTURIZER WITH SPF 30 SUNSCREEN (70764-206)
70764-206-52	2025-01-30	C162847	48780-1	2cef2736-62a0-d83d-e063-dadaa90ab31f	CONTROL CORRECTIVE TINTED MOISTURIZER WITH SPF 30 SUNSCREEN (70764-206)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70764-206-22	CONTROL CORRECTIVE TINTED MOISTURIZERSPF-30 SUNSCREEN	74 mL in 1 TUBE	CREAM	74		5
70764-206-52	CONTROL CORRECTIVE TINTED MOISTURIZERSPF-30 SUNSCREEN	1 in 1 BOX	CREAM	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70764-206	CONTROL CORRECTIVE TINTED MOISTURIZER SPF-30 SUNSCREEN (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [CONTROL CORRECTIVE SKINCARE INC]	4	Current NDC, Legacy NDC, 2 package rows	20230923_8ac09149-f7e7-40a8-b306-98964d0cd6e3.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 289 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 0.5N	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	105651f2-3c99-4ff3-b67b-350a40dc8888	2024-08-06	Warnings	Exact identifier application number: M020
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 0N	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	7b1b551b-e78d-47ff-bb91-0d5f676c73fc	2024-08-06	Warnings	Exact identifier application number: M020
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 0W	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	2411e8e6-a958-4fd9-b5e9-b9a32020ce54	2024-08-06	Warnings	Exact identifier application number: M020
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 1CR	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	062f61d2-a9a7-46e1-92e4-a6bdf257c188	2024-08-06	Warnings	Exact identifier application number: M020
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 1W	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	9c3d513f-8331-4155-a77b-c358093a607c	2024-08-06	Warnings	Exact identifier application number: M020
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 2CR	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	b7f8d1d0-1734-46a5-82fe-b0ac14017522	2024-08-06	Warnings	Exact identifier application number: M020
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 3C	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	c3849d5c-4f91-4147-aeb2-7461a3a94309	2024-08-06	Warnings	Exact identifier application number: M020
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 4C	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	e8f29488-10f8-4df6-b1f5-d9a670f60fca	2024-08-06	Warnings	Exact identifier application number: M020
FOREVER SKIN GLOW 24h wear radiant foundation Perfection and hydration Concentrated floral skincare with suncreen Broad spectrum SPF 15 0CR	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	86e0d1e4-3207-49e6-b5fa-e63f4ca300db	2024-08-06	Warnings	Exact identifier application number: M020
Fruit of the Earth LUV THAT SUN Sport Sunscreen Continuous SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	FRUIT OF THE EARTH, INC.	fd67b009-accc-6c7b-e053-6294a90ad80e	2024-08-06	Warnings	Exact identifier application number: M020
Fruit of the Earth LUV THAT SUN Kids Sunscreen Continuous SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Fruit of the Earth, Inc.	fd67fa5d-f997-c607-e053-6294a90aee2b	2024-08-06	Warnings	Exact identifier application number: M020
Fruit of the Earth LUV THAT SUN Sport Sunscreen Continuous SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	FRUIT OF THE EARTH, INC.	fd66ee9b-5a24-776a-e053-6294a90a6559	2024-08-06	Warnings	Exact identifier application number: M020
SANTO REMEDIOS RADIANCE SILKY MINERAL PRIMER SUNSCREEN SPF 42 IVORY	TITANIUM DIOXIDE, ZINC OXIDE	SANTO REMEDIO LLC	0708ec87-16c4-412b-971b-d4572931c780	2024-08-05	Warnings	Exact identifier application number: M020
EltaMD UV Physical SPF41	ZINC OXIDE AND TITANIUM DIOXIDE SUNSCREEN	CP Skin Health Group, Inc	8fdc04eb-4079-40e3-a1b3-be4a542cf99a	2024-08-05	Warnings	Exact identifier application number: M020
JUNGSAEMMOOL Essential Skin Nuder Longwear Cushion Fair Light	TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE, OCTISALATE	Jungsaemmool Beauty Co., Ltd.	6377c0f7-e2cb-44f0-9786-42c5a9d02f88	2024-08-04	Warnings	Exact identifier application number: M020
JUNGSAEMMOOL Essential Skin Nuder Longwear Cushion Light	TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE, OCTISALATE	Jungsaemmool Beauty Co., Ltd.	e98696d2-7f7f-4a4c-b8ae-849f2d211a04	2024-08-04	Warnings	Exact identifier application number: M020
JUNGSAEMMOOL Essential Skin Nuder Longwear Cushion Medium Deep	TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE, OCTISALATE	Jungsaemmool Beauty Co., Ltd.	f31842f7-3474-4462-87e2-c4ebde97a583	2024-08-04	Warnings	Exact identifier application number: M020
JUNGSAEMMOOL Essential Skin Nuder Longwear Cushion Medium	TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE, OCTISALATE	Jungsaemmool Beauty Co., Ltd.	ccfafefc-fff4-41ff-baf4-3f430c690be7	2024-08-04	Warnings	Exact identifier application number: M020
Alba Botanica Sheer Mineral SPF50	ZINC OXIDE	The Hain Celestial Group, Inc.	f4a02196-288e-1958-e053-2a95a90a5305	2024-07-31	Warnings	Exact identifier application number: M020
Very Emollient Body Daily Shade SPF15	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	The Hain Celestial Group	8eeb25a8-337d-c71b-e053-2995a90a091a	2024-07-31	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
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70764-206-22	70764020622	74 mL in 1 TUBE	74 ml					Historical
70764-206-52	70764020652	1 TUBE in 1 BOX (70764-206-52) / 74 mL in 1 TUBE (70764-206-22)	1 tube	2018-09-11	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
CONTROL CORRECTIVE TINTED MOISTURIZER WITH SPF 30 SUNSCREEN (70764-206)	CONTROL CORRECTIVE SKINCARE INC \| Chemolee Lab Corporation	2025-12-31	HUMAN OTC DRUG LABEL	5