FDA.reportPublic FDA data

HYPOALLERGENIC CBD SENSITIVE SKIN THERAPY Ultra-Lightweight Calming Veil SPF 35

Manufacturer
NV Perricone LLC | Dimensional Merchandising Inc (DMI)
Effective date
2023-09-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:56:07

Label at a glance#

ProductHYPOALLERGENIC CBD SENSITIVE SKIN THERAPY Ultra-Lightweight Calming Veil SPF 35
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration SectionDosage & Administration Section

OTC - ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENTOTC - ACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTSINACTIVE INGREDIENTS

INDICATIONS & USAGE SECTION

INDICATIONS & USAGEINDICATIONS & USAGE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDREN

OTC - PURPOSE SECTION

PURPOSEPURPOSE

WARNINGS SECTION

WARNINGWARNING

RECENT MAJOR CHANGES SECTION

X

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label Principal Display PanelPackage Label Principal Display Panel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
124351b2-6dbf-42d0-9ea7-f0e299215f9aProduct name120210115
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
45634-715-502025-01-30C16284748780-12cef2736-7976-d83d-e063-dadaa90ab31f049e4a9b-3e4f-a3f4-e063-6294a90a302c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
45634-715-50HYPOALLERGENIC CBD SENSITIVE SKIN THERAPY Ultra-Lightweight Calming Veil SPF 3520000 mg in 1 TUBECREAM200002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
45634-715HYPOALLERGENIC CBD SENSITIVE SKIN THERAPY ULTRA-LIGHTWEIGHT CALMING VEIL SPF 35 (ZINC OXIDE) CREAM [NV PERRICONE LLC]21 package rows20230908_049e4a9b-3e4f-a3f4-e063-6294a90a302c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
45634-71545634-715-50

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

Name, UNII, Kind table
NameUNIIKind
LEVOMENOL24WE03BX2TIACT
OCTYLDODECANOL461N1O614YIACT
WATER059QF0KO0RIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ISODODECANEA8289P68Y2IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
GLYCERINPDC6A3C0OXIACT
PROPANEDIOL5965N8W85TIACT
SODIUM CHLORIDE451W47IQ8XIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
PROPYLENE CARBONATE8D08K3S51EIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CANNABIDIOL19GBJ60SN5IACT
XANTHAN GUMTTV12P4NEEIACT
ROSEMARYIJ67X351P9IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
HELIANTHUS ANNUUS FLOWERING TOPBKJ0J3D1BPIACT
TOCOPHEROLR0ZB2556P8IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
STEAROYL GLUTAMIC ACID4R4O71786GIACT
SODIUM BENZOATEOJ245FE5EUIACT
RICE BRANR60QEP13ICIACT
ZINC OXIDESOI2LOH54ZACTIB
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
STEARALKONIUM HECTORITEOLX698AH5PIACT
CASTOR OILD5340Y2I9GIACT
CALCIUM GLUCONATESQE6VB453KIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
TRIHEPTANOIN2P6O7CFW5KIACT
LINGONBERRY0UNK9RZQ7XIACT
DILINOLEIC ACID/BUTANEDIOL COPOLYMER1F2S8T535OIACT
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXIACT
C9-12 ALKANE7J5R5W72QMIACT
GLUCONOLACTONEWQ29KQ9POTIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
04c1538c-2db8-f441-e063-6394a90a3367049e4a9b-3e4f-a3f4-e063-6294a90a302c2023-09-07WarningsExact identifier
spl id: 04c1538c-2db8-f441-e063-6394a90a3367
spl set id: 049e4a9b-3e4f-a3f4-e063-6294a90a302c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.