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 28 of 319 · 6,365 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Biofreeze ProfessionalMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLC00bba5d2-b0e0-701c-e063-6294a90a57412026-05-15WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Overnight Roll-onMENTHOLReckitt Benckiser LLCf67d7b7a-8922-73f6-e053-2995a90a2e802026-05-15WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Overnight ReliefMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLC07be6e88-1850-4d6a-946d-f03830b8c4a22026-05-15WarningsExact identifier
unii: L7T10EIP3A
Biofreeze ProfessionalMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLC6bef9ccb-7a5a-4c67-b1bc-a92b167312da2026-05-15WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Roll-OnMENTHOLReckitt Benckiser LLCebbbe9cb-b1ce-4dac-9fca-f54a2470c4fb2026-05-15WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Precision Relief PenMENTHOLReckitt Benckiser LLCb4cc1db5-a33f-17bc-e053-2995a90ab7eb2026-05-15WarningsExact identifier
unii: L7T10EIP3A
Biofreeze ProfessionalMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLCdb982baf-31ea-4f09-90e3-cd5facb5dfe52026-05-15WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Professional Roll-OnMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLCf62f8ec3-593d-480a-85a0-01fcd7f1790c2026-05-15WarningsExact identifier
unii: L7T10EIP3A
PERFORM COOL AND SOOTHING PAIN RELIEVING ROLL-ONMENTHOLReckitt Benckiser LLC8af185ad-719e-4684-89c0-9c17c12774992026-05-15WarningsExact identifier
unii: L7T10EIP3A
PERFORM COOL and SOOTHING PAIN RELIEVINGMENTHOLReckitt Benckiser LLCef158f63-2d75-47a3-b94a-2d821d5118632026-05-15WarningsExact identifier
unii: L7T10EIP3A
REFRESH LACRI-LUBEMINERAL OIL, PETROLATUMAllergan, Inc.d232a44b-516d-4cdf-a4e7-c3a9a50dc7af2026-05-15WarningsExact identifier
unii: 4T6H12BN9U
Cerave Developed with Dermatologists HealingPETROLATUMLOreal USA Products Incde44ac01-ba17-4f97-ac12-9ea348013bde2026-05-14WarningsExact identifier
unii: 4T6H12BN9U
MELAO Hydrating Lightweight SunscreenOCTOCRYLENE,HOMOSALATE,ETHYLHEXYL SALICYLATE,PHENYLBENZIMIDAZOLE SULFONIC ACID,BUTYL METHOXYDIBENZOYLMETHANE,TITANIUM DIOXIDEGuangdong Aimu Biological Technology Co., Ltd51c353cb-94c4-e110-e063-6394a90a497e2026-05-14WarningsExact identifier
unii: 5A68WGF6WM
unii: V06SV4M95S
unii: G63QQF2NOX
unii: 4X49Y0596W
Plantar Pain Relief PatchLIDOCAINE AND MENTHOLGuangzhou Sumi Technology Innovation Co., Ltd4e8734db-e474-e1fa-e063-6394a90a30292026-05-14WarningsExact identifier
unii: L7T10EIP3A
Hampton Sun SPF 8 Bronze SunscreenHOMOSALATE 7.5%, OCTISALATE 5.00%, AVOBENZONE 3.00%S&C Hampton Sun LLC7cf4d943-be6e-4e38-8891-1e0b22af55362026-05-14WarningsExact identifier
unii: V06SV4M95S
unii: G63QQF2NOX
unii: 4X49Y0596W
SunPlus Healthy Skin Sunny Living SPF 30 Mist SunscreenAVOBENZONE, OCTISALATE, OCTOCRYLENESUNPLUS SKIN CARE LLC9b168046-3536-4ba9-9b5f-4f8c50b8b3542026-05-14WarningsExact identifier
unii: 5A68WGF6WM
unii: G63QQF2NOX
unii: 4X49Y0596W
SunPlus Healthy Skin Sunny Living SPF 50 Mist SunscreenAVOBENZONE, OCTISALATE, OCTOCRYLENESUNPLUS SKIN CARE LLC0e60ecee-d9f4-47e0-92f7-ff319e4422dd2026-05-14WarningsExact identifier
unii: 5A68WGF6WM
unii: G63QQF2NOX
unii: 4X49Y0596W
Hampton Sun SPF 15 SunscreenOCTOCRYLENE 7.50% AVOBENZONE 2.50% OCTISALATE 5.00%S&C Hampton Sun LLC3ce75e74-b5d3-4fbe-8d44-9b6f14f354df2026-05-14WarningsExact identifier
unii: 5A68WGF6WM
unii: G63QQF2NOX
unii: 4X49Y0596W
Target Up and Up SPF 30 Deep Repair Facial Moisturizer SunscreenAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENETARGET CORPORATION51c9bdee-dcff-2818-e063-6294a90abb472026-05-14WarningsExact identifier
unii: 5A68WGF6WM
unii: V06SV4M95S
unii: G63QQF2NOX
unii: 4X49Y0596W
Cold and Heat Lidocaine Patch Plus MentholLIDOCAINE, MENTHOLCardinal Health, 110 dba LEADER77066d01-75b0-4a8d-88d3-c639626d33262026-05-14WarningsExact identifier
unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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