FDA.reportPublic FDA data

Motives Liquid Powder Mineral Foundation SPF 15

Manufacturer
Market America | MANA PRODUCTS, INC. | Mana Products, INC
Effective date
2023-01-25
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-05-31 23:53:28

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Motives Liquid Powder Mineral Foundation SPF 15Motives Liquid Powder Mineral Foundation SPF 15

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
76209-401-032025-01-30C16284748780-12cef2736-813f-d83d-e063-dadaa90ab31fbbf26997-d995-e9e2-e053-2a95a90a7e5c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76209-401-03Motives Liquid Powder Mineral Foundation SPF 1530 g in 1 TUBECREAM3010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76209-401MOTIVES LIQUID POWDER MINERAL FOUNDATION SPF 15 CREAM [MARKET AMERICA]10Legacy NDC, 1 package rows20230126_bbf26997-d995-e9e2-e053-2a95a90a7e5c.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
76209-40176209-401-03

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

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
ea8c4193-83d9-72fe-e053-2a95a90a29e2bbf26997-d995-e9e2-e053-2a95a90a7e5c2023-01-25Exact identifier
spl id: ea8c4193-83d9-72fe-e053-2a95a90a29e2
spl set id: bbf26997-d995-e9e2-e053-2a95a90a7e5c

Reported adverse events (FAERS/openFDA)#

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