FDA.reportPublic FDA data

Motives Liquid Powder Mineral Foundation SPF 15

Manufacturer
MANA PRODUCTS, INC. | MANA Products,INC
Effective date
2021-12-31
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 23:46:12

Label at a glance#

ProductMotives Liquid Powder Mineral Foundation SPF 15
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure1 sections

Label contents#

Full prescribing information#

Motives Liquid Powder Mineral Foundation SPF 15.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Motives Liquid Powder Mineral Foundation SPF 15.jpgMotives Liquid Powder Mineral Foundation SPF 15.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct 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
59735-103-012023-01-30C16284748780-1f386c64a-0896-0266-e053-dadaa90a7c1ab064369d-92fd-51aa-e053-2995a90a24fc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59735-103-01Motives Liquid Powder Mineral Foundation SPF 1530 g in 1 TUBECREAM308

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59735-103MOTIVES LIQUID POWDER MINERAL FOUNDATION SPF 15 CREAM [MANA PRODUCTS, INC.]8Legacy NDC, 1 package rows20220101_b064369d-92fd-51aa-e053-2995a90a24fc.zip

Products#

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

DailyMed product names page 1 of 1 · 38 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59735-10359735-103-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHYTANTRIOL8LVI07A72WIACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5)035JKJ76MTIACT
FERRIC OXIDE RED1K09F3G675IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
POLYGLYCERYL-4 ISOSTEARATE820DPX33S7IACT
MAGNESIUM CHLORIDE02F3473H9OIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
OCTYLDODECANOL461N1O614YIACT
STEARIC ACID4ELV7Z65APIACT
HEXYL LAURATE4CG9F9W01QIACT
CAPRYLYL GLYCOL00YIU5438UIACT
MICAV8A1AW0880IACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
BUTYLENE GLYCOL3XUS85K0RAIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
METHICONE (20 CST)6777U11MKTIACT
TETRAHEXYLDECYL ASCORBATE9LBV3F07AZIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
EDETATE DISODIUM7FLD91C86KIACT
ZINC CHLORIDE86Q357L16BIACT
DIMETHICONE92RU3N3Y1OIACT
ZINC OXIDESOI2LOH54ZACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
LYSINEK3Z4F929H6IACT
HYALURONATE SODIUMYSE9PPT4THIACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)UF7620L1W6IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
HEXYLENE GLYCOLKEH0A3F75JIACT
NYLON-12446U8J075BIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
POTASSIUM CHLORIDE660YQ98I10IACT

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
d47da0c7-8df1-13ea-e053-2a95a90a7bbfb064369d-92fd-51aa-e053-2995a90a24fc2021-12-31Exact identifier
spl id: d47da0c7-8df1-13ea-e053-2a95a90a7bbf
spl set id: b064369d-92fd-51aa-e053-2995a90a24fc

Reported adverse events (FAERS/openFDA)#

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