YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW

Product NDC: 59735-182
11-digit product format: 597350182
Labeler code: 59735
Product ID: 59735-182_4fafb5d1-b38a-dc2e-e063-6394a90a2ce0
Type: HUMAN OTC DRUG
Nonproprietary name: YOUR NAME MINERAL SHEER TINT
Dosage form: CREAM
Route: TOPICAL
Labeler: PML NYC, LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-02-01
Substance: ZINC OXIDE; TITANIUM DIOXIDE
Active strength: 5; 5 g/30mL; g/30mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 5 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	59735-182		I	Inactivated by FDA	2026-10-16
excluded package	package	59735-182	59735-182-01	I	Inactivated by FDA	2026-10-16
excluded package	package	59735-182	59735-182-04	I	Inactivated by FDA	2026-10-16
excluded package	package	59735-182	59735-182-06	I	Inactivated by FDA	2026-10-16
excluded package	package	59735-182	59735-182-08	I	Inactivated by FDA	2026-10-16

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: YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	5 g/30mL
TITANIUM DIOXIDE	5 g/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
SOI2LOH54Z	Internal UNII lookup
15FIX9V2JP	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
316c5d69-46f4-7677-e063-6294a90a610f	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
9e37788c-b1bf-42ae-aac9-b60601606144	Product name	8	20260122
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515
1527ac37-808d-43be-a63e-74e1258dbe46	Product name	9	20250219
bed0530e-f939-4541-956b-6928a2f6404f	Product name	1	20241008
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	6	20240814
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5	Product name	8	20230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
0ec3537a-6c9b-432a-896c-b9ea8723049a	Product name	9	20200701
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cd	Product name	2	20190619
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
7916de40-e296-41f0-b811-6d0df1a33e2c	Product name	9	20180627
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	2	20171212
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
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
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
684ea482-2e8b-14af-5664-b98f1e402036	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
b060cc1a-fe47-856b-0b77-4448b5963de8	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
59735-182-01	YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW
59735-182-04	YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW
59735-182-06	YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW
59735-182-08	YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
59735-182-09	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	30 mL in 1 TUBE	CREAM	30	8
59735-182-10	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	1 in 1 CARTON	CREAM	1	8
59735-182-01	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	30 mL in 1 TUBE	CREAM	30	6
59735-182-01	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	1 in 1 CARTON	CREAM	1	6
59735-182-03	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	30 mL in 1 TUBE	CREAM	30	6
59735-182-04	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	1 in 1 CARTON	CREAM	1	6
59735-182-05	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	30 mL in 1 TUBE	CREAM	30	6
59735-182-06	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	1 in 1 CARTON	CREAM	1	6
59735-182-07	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	30 mL in 1 TUBE	CREAM	30	6
59735-182-08	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW	1 in 1 CARTON	CREAM	1	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59735-182	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW (YOUR NAME MINERAL SHEER TINT) CREAM [MANA PRODUCT, INC]	7	Current NDC, 2 package rows	20250331_316c5d69-46f4-7677-e063-6294a90a610f.zip
59735-182	YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW (YOUR NAME MINERAL SHEER TINT) CREAM [MANA PRODUCT, INC]	6	Current NDC, 8 package rows	20240808_0e24934c-b25e-51ef-e063-6394a90a2e3f.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 57 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Bath and Body Works SPF At The Beach	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Bath & Body Works, Inc.	1c315bdb-dc33-1737-e063-6294a90a31a4	2026-03-02	Warnings	Exact identifier application number: M020
Bath and Body Works SPF Tahiti Isle	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Bath & Body Works, Inc.	38d02c8d-cdc8-b8d6-e063-6294a90ad9e4	2026-03-02	Warnings	Exact identifier application number: M020
Sport	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTISALATE	Old East Main Co.	a460e512-f268-4941-beb6-29df10fdbb3a	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Tanning Sunscreen SPF 15	AVOBENZONE HOMOSALATE OCTISALATE	Old East Main Co.	42258ebe-e3cc-4d70-e063-6294a90a9651	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALAT, OCTOCRYLENE	Old East Main Co.	db876d34-1af9-4e0a-9e9a-32a8b00e9405	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Sunscreen	AVOBENZONE, HOMOSALATE,OTISALATE, OCTOCRYLENE	Old East Main Co.	2ea288fe-815d-4568-9592-55ea428448fa	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	cea1c223-c9d4-42ac-8c5b-c0ca647d57a1	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Old East Main Co.	00ee1dc6-b4f3-4ae3-890c-8e37f6d3fe3a	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	8f4a6a31-2fae-42fe-924f-10237c59e791	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	ef48288b-533f-4924-ba12-fc8cb83643d4	2026-03-02	Warnings	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	e6976bf4-ad77-4953-858f-4a0ec7f4300c	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	b3d2da09-d9c9-4c27-82fe-a434ece2f099	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	ba9331ef-3744-4072-80a2-af95c6f7ee05	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	4a0cab2d-3c73-4b0b-b0c4-f72b1a0de1cf	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	1a53d8d5-e650-4825-8a3b-7cf42c36e3e5	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	086dfda5-9fe7-46b4-9964-4977b86cfdd5	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Old East Main Co.	ce9a2139-c5c2-43e2-bd51-1f14ace594d9	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M020
Bask SPF 40 Broad Spectrum	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Surfside Skincare, Inc. dba Bask Suncare	49a30877-e39f-46a3-e063-6394a90a8dd2	2026-03-02	Warnings	Exact identifier application number: M020
Sunscreen SPF30	AVOBENZONE 3% HOMOSALATE 10% OCTOCRYLENE 5%	Worthy Promotional Products	f6014a97-12d3-4f42-86de-866a206c6c06	2026-03-02	Warnings	Exact identifier application number: M020
2000DL-CL30V	SPF30 BS VANILLA	Epic Laboratories, LLC	02488aad-28be-4ffb-e063-6294a90ad01e	2026-03-02	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
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
59735-182-01	59735018201	30 mL in 1 TUBE	30 ml				Historical
59735-182-03	59735018203	30 mL in 1 TUBE	30 ml				Historical
59735-182-04	59735018204	1 in 1 CARTON					Historical
59735-182-05	59735018205	30 mL in 1 TUBE	30 ml				Historical
59735-182-06	59735018206	1 in 1 CARTON					Historical
59735-182-07	59735018207	30 mL in 1 TUBE	30 ml				Historical
59735-182-08	59735018208	1 in 1 CARTON					Historical
59735-182-09	59735018209	30 mL in 1 TUBE	30 ml				Historical
59735-182-10	59735018210	1 TUBE in 1 CARTON (59735-182-10) / 30 mL in 1 TUBE (59735-182-09)	1 tube	2011-02-01	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW	PML NYC, LLC	2026-04-17	HUMAN OTC DRUG LABEL	8
YOUR NAME MINERAL SHEER TINT BROAD SPECTRUM SPF 20- SUN GLOW	Mana Product, Inc \| Mana Products,Inc \| Mana Products, Inc	2024-08-05	HUMAN OTC DRUG LABEL	6