WHAMISA ORGANIC PEAR BLOSSOM SUNSCREEN

Product NDC: 73391-0101
11-digit product format: 733910101
Labeler code: 73391
Product ID: 73391-0101_4dab3334-793e-a534-e063-6394a90a1efe
Type: HUMAN OTC DRUG
Nonproprietary name: ZINC OXIDE
Dosage form: CREAM
Route: TOPICAL
Labeler: ENS KOREA Co., Ltd.
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-05-30
Substance: ZINC OXIDE
Active strength: 24.05 g/100g
NDC exclude flag: No
Listing certified through: 2027-12-31
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: WHAMISA ORGANIC PEAR BLOSSOM SUNSCREEN
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	24.05 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
15FIX9V2JP	Internal UNII lookup
O414PZ4LPZ	Internal UNII lookup
SOI2LOH54Z	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
417424	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
34f9688d-efa1-1d3f-e063-6294a90ab127	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73391-0101-1	WHAMISA ORGANIC PEAR BLOSSOM SUNSCREEN	50 g in 1 TUBE	CREAM	50		3
73391-0101-2	WHAMISA ORGANIC PEAR BLOSSOM SUNSCREEN	1 in 1 PACKAGE	CREAM	1		3

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 142 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mineral Sunscreen Dry Touch NT	TITANIUM DIOXIDE, ZINC OXIDE	Cutis Wellness Dermatology And Dermatopathology PLLC	334ffc49-3196-0995-e063-6394a90ad559	2025-12-09		Exact identifier application number: M020
Foam Weightless Sunscreen Non-Tinted Drytouch NT	TITANIUM DIOXIDE, ZINC OXIDE	Cutis Wellness Dermatology And Dermatopathology PLLC	335ec22c-6a9a-c4d1-e063-6394a90ac0b0	2025-12-09		Exact identifier application number: M020
Mineral Sunscreen Moisturizing Non-Tinted	ZINC OXIDE	Cutis Wellness Dermatology And Dermatopathology PLLC	3360a208-5f17-a74b-e063-6294a90a13e1	2025-12-09		Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Lily Lee, MD	323356ea-31a0-6ff0-e063-6294a90a135c	2025-12-09		Exact identifier application number: M020
Non-Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Lily Lee, MD	32330376-5db0-202b-e063-6294a90add15	2025-12-09		Exact identifier application number: M020
Sunscreen Plus Untinted	ZINC OXIDE	Lily Lee, MD	32354468-94a2-604b-e063-6394a90adfb5	2025-12-09		Exact identifier application number: M020
Sunscreen Plus Tinted	ZINC OXIDE	Lily Lee, MD	32346536-f542-ef0f-e063-6394a90a0464	2025-12-09		Exact identifier application number: M020
Sunscreen Plus Mineral Stick Untinted	TITANIUM DIOXIDE, ZINC OXIDE	Lily Lee, MD	3234b498-5b56-55f4-e063-6294a90a9b87	2025-12-09		Exact identifier application number: M020
Sunscreen Plus Tinted	ZINC OXIDE	Lily Lee, MD	3235a696-92aa-788c-e063-6394a90a0149	2025-12-09		Exact identifier application number: M020
Sunscreen Plus Mineral Stick Tinted	TITANIUM DIOXIDE, ZINC OXIDE	Lily Lee, MD	32351db0-884c-8fa0-e063-6294a90acba2	2025-12-09		Exact identifier application number: M020
Sunscreen Plus Untinted	ZINC OXIDE	Lily Lee, MD	3235786d-7ba9-c9ab-e063-6294a90a7f2e	2025-12-09		Exact identifier application number: M020
Tinted Mineral Sunscreen 20% Zinc Oxide	ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	31416d04-2d6f-7cf9-e063-6294a90a9806	2025-12-09	Warnings	Exact identifier application number: M020
Matte Invisible Mineral Sunscreen Non-Tinted	ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	3143968a-096e-b9ac-e063-6294a90ada0d	2025-12-09	Warnings	Exact identifier application number: M020
Daily Mineral Sunscreen 20% Zinc Oxide	ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	314299b1-a78b-c1bd-e063-6294a90ab43b	2025-12-09	Warnings	Exact identifier application number: M020
Sheer Satin Mineral Sunscreen Tinted	TITANIUM DIOXIDE, ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	3143d8b0-4af8-f52d-e063-6294a90a926b	2025-12-09	Warnings	Exact identifier application number: M020
Matte Invisible Mineral Sunscreen	ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	3142ed0f-f379-f240-e063-6294a90a5303	2025-12-09	Warnings	Exact identifier application number: M020
Sheer Non-Tinted Mineral Sunscreen Stick	TITANIUM DIOXIDE, ZINC OXIDE	Face Collection, L.L.C.	33d83cfb-045d-141c-e063-6394a90a2e04	2025-12-09		Exact identifier application number: M020
First Aid Beauty FAB Ultra Light Mineral Sunscreen Broad Spectrum SPF 30	ZINC OXIDE	The Procter & Gamble Manufacturing Company	45875865-5e9c-d652-e063-6394a90ad5fa	2025-12-09	Warnings	Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Maloney Plastic Surgery Skin Care, PLLC	316b7584-c782-fe9e-e063-6394a90a76fe	2025-12-09		Exact identifier application number: M020
Transparent Tinted Mineral Sunscreen Stick	TITANIUM DIOXIDE, ZINC OXIDE	Face Collection, L.L.C.	33dbfd9b-b90f-bb32-e063-6294a90af7dc	2025-12-09		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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
417424	salicylic acid 1 % Topical Cream	PSN	34f9688d-efa1-1d3f-e063-6294a90ab127	3
417424	salicylic acid 10 MG/ML Topical Cream	SCD	34f9688d-efa1-1d3f-e063-6294a90ab127	3
417424	salicylic acid 1 % Topical Cream	SY	34f9688d-efa1-1d3f-e063-6294a90ab127	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
73391-0101-1	73391010101	50 g in 1 TUBE	50 g				Historical
73391-0101-2	73391010102	1 TUBE in 1 PACKAGE (73391-0101-2) / 50 g in 1 TUBE (73391-0101-1)	1 tube	2025-05-30	Yes	No	Current