NDC 11697-462-01 - Forever Sun Lips

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
11697-462
Requested NDC
11697-462-01
Package NDCs from labels
11697-462-01, 11697-462-02, 11697-462-03
Manufacturer
Aloe Vera of America, Inc.
Effective date
2014-03-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Forever Sun LipsAloe Vera of America, Inc.2014-03-25HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11697-462-032019-11-27C16284748780-19855e2a2-50eb-60a7-e053-dbdaa90a05bdForever Sun Lips

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11697-462-01Forever Sun Lips4.25 g in 1 TUBELIPSTICK4.251
11697-462-02Forever Sun Lips1 in 1 CARTONLIPSTICK11
11697-462-03Forever Sun Lips12 in 1 BOXLIPSTICK121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11697-462FOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1Legacy NDC, 3 package rows20140425_dd7ccc7b-ebeb-4a24-9f69-f78adcede0fc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOXFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
HOMOSALATEACTIVE INGREDIENTV06SV4M95SFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
OCTISALATEACTIVE INGREDIENT4X49Y0596WFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
OCTOCRYLENEACTIVE INGREDIENT5A68WGF6WMFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
PETROLATUMACTIVE INGREDIENT4T6H12BN9UFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
AVOBENZONEACTIVE MOIETYG63QQF2NOXFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
HOMOSALATEACTIVE MOIETYV06SV4M95SFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
OCTISALATEACTIVE MOIETY4X49Y0596WFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
OCTOCRYLENEACTIVE MOIETY5A68WGF6WMFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
PETROLATUMACTIVE MOIETY4T6H12BN9UFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
ALLANTOININACTIVE INGREDIENT344S277G0ZFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
BUTYLOCTYL SALICYLATEINACTIVE INGREDIENT2EH13UN8D3FOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
CANDELILLA WAXINACTIVE INGREDIENTWL0328HX19FOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
CERESININACTIVE INGREDIENTQ1LS2UJO3AFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
ETHYLHEXYL HYDROXYSTEARATEINACTIVE INGREDIENTB7I80BVV5EFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
JOJOBA OILINACTIVE INGREDIENT724GKU717MFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
MENTHOLINACTIVE INGREDIENTL7T10EIP3AFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
MENTHYL LACTATE, (-)-INACTIVE INGREDIENT2BF9E65L7IFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
SOYBEAN OILINACTIVE INGREDIENT241ATL177AFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1
YELLOW WAXINACTIVE INGREDIENT2ZA36H0S2VFOREVER SUN LIPS (SUNSCREEN) LIPSTICK [ALOE VERA OF AMERICA, INC.]1

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 30 of 319 · 6,365 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BiofreezeMENTHOLReckitt Benckiser LLC684faf63-5e44-4471-8384-e8fa7c0d842a2026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLC4c798b06-6ee5-41d1-8a14-f6889512ade32026-05-13WarningsExact identifier
unii: L7T10EIP3A
BIOFREEZEMENTHOLReckitt Benckiser LLC83d5c2f2-2413-4d28-83b2-0808d0917b4d2026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLC10a8face-47da-ebbe-e063-6294a90a42fe2026-05-13WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Foot CreamMENTHOLReckitt Benckiser LLC32450cbf-4ed4-402b-a30e-e08a17bba3fb2026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLCa227213b-e89f-7144-e053-2a95a90a7e742026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLC00bb462a-27d0-6f74-e063-6394a90a90ec2026-05-13WarningsExact identifier
unii: L7T10EIP3A
BioFreeze Dry StickMENTHOLReckitt Benckiser LLC26d62cd2-9209-8cca-e063-6394a90a20282026-05-13WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Colorless Roll-OnMENTHOLReckitt Benckiser LLCa8d59d45-0e85-43d1-affd-bbe922c4acb12026-05-13WarningsExact identifier
unii: L7T10EIP3A
Biofreeze ColorlessMENTHOLReckitt Benckiser LLC939dbbc3-71ec-4990-840e-7c9b8d4305622026-05-13WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Flexible Relief StripMENTHOLReckitt Benckiser LLC6ec26bae-e395-49aa-969e-8c653d6f0b272026-05-13WarningsExact identifier
unii: L7T10EIP3A
Biofreeze FoamMENTHOLReckitt Benckiser LLC890191e8-99ad-489c-8f21-2592f3d319362026-05-13WarningsExact identifier
unii: L7T10EIP3A
Standard Procedure SPF 50 Sunscreen Face and BodyAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEBaxter Laboratories34f6150d-9627-94a5-e063-6394a90ad4482026-05-13WarningsExact identifier
unii: 5A68WGF6WM
unii: V06SV4M95S
unii: G63QQF2NOX
unii: 4X49Y0596W
Valtrum TOPICAL ANALGESICCAMPHOR, MENTHOL, METHYL SALICYLATELaboratorios Quantium LLCf3c4cc3a-f3a3-4d02-97e0-9c3fc1a67c3e2026-05-13WarningsExact identifier
unii: L7T10EIP3A
CeraVe Developed with Dermotologists Ultra Light Moisturizing Broad Spectrum SPF 30AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENEL'Oreal USA Products Incdefa9588-95be-4f5c-86bb-53d6a1df7f5f2026-05-13WarningsExact identifier
unii: 5A68WGF6WM
unii: V06SV4M95S
unii: G63QQF2NOX
unii: 4X49Y0596W
Biofreeze Professional ColorlessMENTHOL, UNSPECIFIED FORMReckitt Benckiser4639201c-a67a-475f-8df6-3dc6225803ad2026-05-12WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Professional Colorless Roll-OnMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLCbae9946a-4c68-4759-9fb3-0a61a7ad0eb72026-05-12WarningsExact identifier
unii: L7T10EIP3A
Frase Skin SPF 30 Face Sunscreen Activated Vitamin D TechnologyAVOBENZONE, OCTISALATE, OCTOCRYLENEFrase Skin PTY LTDd904fd23-a3a1-4564-8eec-13a4c96e23f72026-05-12WarningsExact identifier
unii: 5A68WGF6WM
unii: G63QQF2NOX
unii: 4X49Y0596W
Cancer Council Daily Face Moisturizer SPF50AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEVitality US Co.1b4333b8-5747-c591-e063-6294a90a99242026-05-12WarningsExact identifier
unii: 5A68WGF6WM
unii: V06SV4M95S
unii: G63QQF2NOX
unii: 4X49Y0596W
Instaflex Pain Relief CreamMENTHOLHealthy Directions, LLC665b847a-9cfb-49fc-975b-81c97f9365752026-05-12WarningsExact identifier
unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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