RAIN AND SHINE LIPTINT

Manufacturer
ORIGINS NATURAL RESOURCES INC | ESTEE LAUDER COSMETICS, LTD | ESTEE LAUDER N.V. | Len-Ron Manufacturing Division of Aramis Inc. | Aramis Inc. | Northtec Bristol | Northtec Keystone | PADC 1 | Estee Lauder Pennsylvania Distribution Center 2 | Estee Lauder Cosmetics, Ltd. | Estee Lauder Cosmetics Distribution Center | Estee Lauder Kabushiki Kaisha | Whitman Laboratories Ltd. | Aveda Corporation
Effective date
2010-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:14

Label at a glance#

ProductRAIN AND SHINE LIPTINT WITH SPF 10 SUNSCREEN
Active ingredientOCTINOXATE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: OCTINOXATE 3.5%

WARNINGS SECTION

WARNING: STOP USE IF IRRITATION OCCURS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL


ORIGINS

RAIN AND SHINE

LIP TINT WITH SPF 10 SUNSCREEN


NET WT 0.9 OZ / 2.5 GM


ORIGINS NAT. RES. DISTR.

NEW YORK, NY 10022


FOLDING CARTON
FOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59427-728-012019-10-21C16284748780-1956f9ecf-de27-621f-e053-dbdaa90a74ad6e510db9-4253-4813-9a4d-2399d722d5bb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59427-728-01RAIN AND SHINE LIPTINTWITH SPF 10 SUNSCREEN1 in 1 CARTONLIPSTICK11
59427-728-02RAIN AND SHINE LIPTINTWITH SPF 10 SUNSCREEN2.5 g in 1 CARTRIDGELIPSTICK2.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59427-728RAIN AND SHINE LIPTINT WITH SPF 10 SUNSCREEN (OCTINOXATE) LIPSTICK [ORIGINS NATURAL RESOURCES INC]1Legacy NDC, 2 package rows20100415_6e510db9-4253-4813-9a4d-2399d722d5bb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTINOXATEACTIVE MOIETY4Y5P7MUD511

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59427-72859427-728-02, 59427-728-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB

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
196e19b5-ae01-44cd-817c-da1c28735d606e510db9-4253-4813-9a4d-2399d722d5bb2010-04-13WarningsExact identifier
spl id: 196e19b5-ae01-44cd-817c-da1c28735d60
spl set id: 6e510db9-4253-4813-9a4d-2399d722d5bb

Reported adverse events (FAERS/openFDA)#

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