FDA.reportPublic FDA data

Nutrascreen

Manufacturer
Danne Montague King
Effective date
2024-07-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:15:37

Label at a glance#

ProductNutrascreen
Active ingredientZINC OXIDE
Label structure12 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

See description image attached.See description image attached.

INACTIVE INGREDIENT SECTION

See Inactive Ingredients image attached.See Inactive Ingredients image attached.

INSTRUCTIONS FOR USE SECTION

See directions image attached.See directions image attached.

OTC - ACTIVE INGREDIENT SECTION

See active ingredient image attached.edSee active ingredient image attached.ed

OTC - PURPOSE SECTION

See purpose image attached.See purpose image attached.

OTC - QUESTIONS SECTION

Call toll free 1-888-DANNE-4-UCall toll free 1-888-DANNE-4-U

OTHER SAFETY INFORMATION

Exclusive formula provides increased dermal hydration and improves the skin's overall appearance. Keep product from excessive heat and away from direct sun.Exclusive formula provides increased dermal hydration and improves the skin's overall appearance. Keep product from excessive heat and away from direct sun.

WARNINGS SECTION

see attached warnings imagesee attached warnings image

INDICATIONS & USAGE SECTION

See uses image attached.See uses image attached.

DOSAGE & ADMINISTRATION SECTION

Directions: apply generously 15 minutes before sun exposure. reapply: after 80 minutes of swimming or sweating. immediately after towel drying. at least every 2 hours.Directions: apply generously 15 minutes before sun exposure. reapply: after 80 minutes of swimming or sweating. immediately after towel drying. at least every 2 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings: (For external use only) ... Keep out of reach of children.Warnings: (For external use only) ... Keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DMK NUTRASCREENDMK NUTRASCREEN

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81537-102-012026-01-29C16284748780-149896155-c616-586f-e063-e6dba90add90Nutrascreen SPF 30
81537-102-022026-01-29C16284748780-149896155-c616-586f-e063-e6dba90add90Nutrascreen SPF 30
81537-102-032026-01-29C16284748780-149896155-c616-586f-e063-e6dba90add90Nutrascreen SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81537-102-01Nutrascreen15 mL in 1 BOTTLE, PUMPLOTION152
81537-102-02Nutrascreen50 mL in 1 BOTTLE, PUMPLOTION502
81537-102-03Nutrascreen120 mL in 1 BOTTLE, PUMPLOTION1202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81537-102NUTRASCREEN (REPLENISH AND PROTECT DAY CREAM) LOTION [DANNE MONTAGUE KING]23 package rows20240720_06e86339-8bb0-2eac-e063-6394a90acde8.zip

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81537-10281537-102-01, 81537-102-02, 81537-102-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUNFLOWER OIL3W1JG795YIIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
ALTEROMONAS MACLEODII POLYSACCHARIDESAP6XG2GR8ZIACT
CYCLOMETHICONE 6XHK3U310BAIACT
CYCLOMETHICONE 50THT5PCI0RIACT
SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S)5F4963KLHSIACT
ZINC OXIDESOI2LOH54ZACTIB
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER9NH1UDD2RRIACT
TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONEX75PL53TZJIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
TOCOPHEROLR0ZB2556P8IACT
WATER059QF0KO0RIACT
SEA SALT87GE52P74GIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHOSPHATIDYLCHOLINE, SOYBEAN1T6N4D9YV6IACT
ISOHEXADECANE918X1OUF1EIACT
POLYSORBATE 806OZP39ZG8HIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
STEAROYL INULINWKJ43CL46DIACT
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S)RLA2U05Z4QIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM LEVULINATEVK44E1MQU8IACT
SODIUM ANISATEF9WFJ28MV9IACT
PROPANEDIOL5965N8W85TIACT
GLYCERINPDC6A3C0OXIACT
PENTYLENE GLYCOL50C1307PZGIACT
POLYGONUM AVICULARE WHOLEM990N03611IACT

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
1d9c84c2-11eb-726e-e063-6294a90a8c7c06e86339-8bb0-2eac-e063-6394a90acde82024-07-19WarningsExact identifier
spl id: 1d9c84c2-11eb-726e-e063-6294a90a8c7c
spl set id: 06e86339-8bb0-2eac-e063-6394a90acde8

Reported adverse events (FAERS/openFDA)#

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