Sage and Zinc Facial Hydrating SPF15

Product NDC: 76293-372
11-digit product format: 762930372
Labeler code: 76293
Product ID: 76293-372_c082be90-3333-41de-9e24-6ee3d073e18b
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: LOTION
Route: TOPICAL
Labeler: Emeis Cosmetics Pty Ltd
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-01-01
Substance: ZINC OXIDE
Active strength: 195 mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: Sage and Zinc Facial Hydrating SPF15
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	195 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
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
ccabd647-ecdd-7230-e053-2a95a90a7a96	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2	Product name	5	20250304
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
baf7f49c-75b6-496b-a00e-8e766a8e4f03	Product name	1	20210127
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76293-372-01	Sage and Zinc Facial Hydrating SPF15	57 g in 1 BOTTLE, PUMP	LOTION	57		3
76293-372-01	Sage and Zinc Facial Hydrating SPF15	1 in 1 CARTON	LOTION	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76293-372	SAGE AND ZINC FACIAL HYDRATING SPF15 (ZINC OXIDE) LOTION [EMEIS COSMETICS PTY LTD]	2	Current NDC, Legacy NDC, 2 package rows	20241024_ccabd647-ecdd-7230-e053-2a95a90a7a96.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 202 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dolce and Gabbana Everlast Foundation SPF 20 11W Light Medium	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	303967d1-9df8-4a8e-a264-6b0d8fdbf2a8	2025-08-05	Warnings	Exact identifier application number: M020
Dolce and Gabbana Everlast Foundation SPF 20 12N Light Medium	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	26062cd7-3817-46c7-b65f-92cd57eca5dd	2025-08-05	Warnings	Exact identifier application number: M020
Dolce and Gabbana Everlast Foundation SPF 20 13C Light Medium	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	448a24a3-91ef-4530-828c-e77d8aae7f0b	2025-08-05	Warnings	Exact identifier application number: M020
JORDAN FAT KIDS Tallow Sunscreen SPF 30	MENTHOL, METHYL SALICYLATE	JORDAN FAT KIDS LLC	72ac88cf-9f20-44ea-b3a2-12c922eec2b3	2025-08-04	Warnings	Exact identifier application number: M020
Dolce and Gabbana Everlast Foundation SPF 20 02C Light	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	09f9e59b-6f71-4d42-9b5d-275f756d985b	2025-08-04	Warnings	Exact identifier application number: M020
Dolce and Gabbana Everlast Foundation SPF 20 03W Light	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	3b1e4480-8409-425e-b98d-eb4dcf2471e8	2025-08-04	Warnings	Exact identifier application number: M020
Dolce and Gabbana Everlast Foundation SPF 20 06W Light	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	3090422e-fc18-45b8-88f2-6a9b282a7205	2025-08-04	Warnings	Exact identifier application number: M020
Dolce and Gabbana Everlast Foundation SPF 20 05N Light	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	f93aa5d2-90ab-4e11-874e-2ede4b25c4b6	2025-08-04	Warnings	Exact identifier application number: M020
Dolce and Gabbana Everlast Foundation SPF 20 04C Light	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	f055cd51-7b1d-43df-8990-8f60ba1eb91c	2025-08-04	Warnings	Exact identifier application number: M020
Dolce and Gabbana Everlast Foundation SPF 20 07N Light	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	d4c76bc5-205b-45fd-8a02-4f4b17458503	2025-08-04	Warnings	Exact identifier application number: M020
AHAVA Extreme Daily Firmness And Protection Broad Spectrum SPF30	HOMOSALATE, OCTISALATE, AVOBENZONE, ENSULIZOLE, AND OCTOCRYLENE	AHAVA Dead Sea Laboratories Ltd	b22af9ef-4b69-4e70-a65d-f421e1d178af	2025-08-01	Warnings	Exact identifier application number: M020
Neutrogena Collagen Bank SPF Moisturizer Broad Spectrum SPF 30 and Neutrogena Collagen Bank Moisturizer	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Kenvue Brands LLC	3b4dbc5a-0754-0e71-e063-6394a90aa63c	2025-08-01	Warnings	Exact identifier application number: M020
Kids Tallow Sunscreen SPF50	NON-NANO ZINC OXIDE 25%	FOUNDATION COMMERCE INC	3b4eca91-965f-66c6-e063-6394a90a78ca	2025-08-01	Warnings	Exact identifier application number: M020
Vigority Tallow Sunscreen SPF30	NON-NANO ZINC OXIDE 19%	FOUNDATION COMMERCE INC	3b4f5941-15ae-a760-e063-6394a90a2abe	2025-08-01	Warnings	Exact identifier application number: M020
Pipette Mineral Sunscreen SPF 50	ZINC OXIDE	Pipette LLC	3a10657a-bc16-181d-e063-6294a90a485b	2025-08-01	Warnings	Exact identifier application number: M020
No7 Restore and Renew Face and Neck Multi Action Day Cream Sunscreen Broad Spectrum SPF 30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	BCM Cosmetique SAS	3f0500cc-013b-7069-e063-6294a90a1a5f	2025-08-01	Warnings	Exact identifier application number: M020
Daily Antioxidant Mineral Sunscreen	ZINC OXIDE	MONIKA G KIRIPOLSKY MD INC.	3b3d7ff2-1463-8d8e-e063-6394a90a5ac8	2025-07-31	Warnings	Exact identifier application number: M020
Shaklee Shield Sheer Mineral Body Sunscreen SPF 30	ZINC OXIDE	Shaklee Corp	c9b8e04c-11ee-4c4f-8693-aa4dc6e66aca	2025-07-31	Warnings	Exact identifier application number: M020
Equate SUNSCREEN spf 50 SPORT broadspectrum	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Walmart	4e5280b2-1437-4d97-bb4c-db1a1632fea7	2025-07-31	Warnings	Exact identifier application number: M020
Tallow Sunscreen SPF 30	NON-NANO ZINC OXIDE 19%	FOUNDATION COMMERCE INC	3b410ed7-c629-e39c-e063-6294a90a12f6	2025-07-31	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
76293-372-01	76293037201	1 BOTTLE, PUMP in 1 CARTON (76293-372-01) / 57 g in 1 BOTTLE, PUMP	2022-01-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Sage & Zinc Facial Hydrating Lotion SPF15	Emeis Cosmetics Pty Ltd \| Ensign Laboratories Proprietary Limited	2025-12-18	HUMAN OTC DRUG LABEL	3