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 98 of 315 · 6,300 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mugwort Patch (Lumbar spine use)2%MENTHOLYIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED478e4b21-6d81-4cd3-e063-6394a90a18fe2026-01-04WarningsExact identifier
unii: L7T10EIP3A
Mugwort Patch (Knee use)2%MENTHOLYIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED478e86d2-3030-91eb-e063-6394a90a4db02026-01-04WarningsExact identifier
unii: L7T10EIP3A
Skin Protectant for Babies and kidsSKIN PROTECTANT OINTMENTNeilmed Pharmaceuticals Inc.448b70db-ca81-db7b-e063-6294a90a5f0d2026-01-02WarningsExact identifier
unii: 4T6H12BN9U
HyVee Cough Drops CherryMENTHOLXiamen Kang Zhongyuan Biotechnology Co., Ltd.c5b11a9c-6d93-4772-93c2-1ef5c56470162026-01-02WarningsExact identifier
unii: L7T10EIP3A
HyVee Cough Drops Honey LemonMENTHOLXiamen Kang Zhongyuan Biotechnology Co., Ltd.fae96736-1453-42fe-8158-cde770b231652026-01-02WarningsExact identifier
unii: L7T10EIP3A
HyVee Cough Drops MentholMENTHOLXiamen Kang Zhongyuan Biotechnology Co., Ltd.8cac1229-8e8e-4d8c-9f18-c2cd0f6f50bd2026-01-02WarningsExact identifier
unii: L7T10EIP3A
Doctor Hoys Pain Relief GelMENTHOL, CAMPHOR (SYNTHETIC)Dynamic Blending Specialists, Inc.50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a82026-01-02WarningsExact identifier
unii: L7T10EIP3A
Doctor Hoys Pain Relief Gel Roll-OnMENTHOL, CAMPHOR (SYNTHETIC)Dynamic Blending Specialists, Inc.bf47acb2-6c90-4d5c-820b-447cac9305a42026-01-02WarningsExact identifier
unii: L7T10EIP3A
Menthozen CreamMETHYL SALICYLATE, MENTHOL, CAPSAICINVillage Pharma LLC63bb0283-cfbe-4e9c-8772-73062c0c8d052026-01-01WarningsExact identifier
unii: L7T10EIP3A
Menthozen HydrogelMENTHOL, CAPSAICINVillage Pharma LLC4c979a71-7c8f-4dff-abae-bf4cdf8f67b42026-01-01WarningsExact identifier
unii: L7T10EIP3A
Lidozen GelLIDOCAINE HYDROCHLORIDE, MENTHOLVillage Pharma LLCffb7831f-4ca9-4d73-8303-e9cd900789822026-01-01WarningsExact identifier
unii: L7T10EIP3A
OKeeffes Lip RepairAVOBENZONE, DIMETHICONE, OCTINOXATE, OCTOCRYLENEThe Gorilla Glue Company/O'Keeffe's Company6805b3e9-77cb-bfee-e053-2991aa0a8d982026-01-01WarningsExact identifier
unii: 5A68WGF6WM
unii: G63QQF2NOX
MenthozenMETHYL SALICYLATE, MENTHOL, CAPSAICINVillage Pharma LLC48b1b99e-d0ec-4e5c-b80c-c0d2d87ecb132026-01-01WarningsExact identifier
unii: L7T10EIP3A
Walgreens 50 Pina Colada Scented SunscreenAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEWALGREEN COMPANY4978c811-be34-9fc3-e063-6394a90a2d802026-01-01WarningsExact identifier
unii: 5A68WGF6WM
unii: V06SV4M95S
unii: G63QQF2NOX
unii: 4X49Y0596W
Unicorn Snot 35 SPF Glitter Spritz rose gold shimmerAVOBENZONE, OCTISALATE, OCTOCRYLENEJailbreak Toys, Inc. DBA UNICORN SNOT498b7c1a-e66d-9736-e063-6394a90a47122026-01-01WarningsExact identifier
unii: 5A68WGF6WM
unii: G63QQF2NOX
unii: 4X49Y0596W
No7 Lift and Luminate Triple Action Day Cream SPF 30AVOBENZONE, OCTISALATE, OCTOCRYLENEBCM Ltdf7d5aa8a-9f4a-426b-ac9d-9690cf0103e02026-01-01WarningsExact identifier
unii: 5A68WGF6WM
unii: G63QQF2NOX
unii: 4X49Y0596W
NUVALU 100 PURE PETROLEUMWHITE PETROLATUMJC SALES48f74b99-7ead-b0d0-e063-6394a90a49292026-01-01WarningsExact identifier
unii: 4T6H12BN9U
NUVALU PETROLEUM BABY FRESH SCENTWHITE PETROLATUMJC SALES48f79c2a-b314-169f-e063-6294a90a576e2026-01-01WarningsExact identifier
unii: 4T6H12BN9U
NUVALU PETROLEUM BABY FRESH SCENTWHITE PETROLATUMJC SALES490ac0a6-eac0-a74f-e063-6394a90a84ed2026-01-01WarningsExact identifier
unii: 4T6H12BN9U
NUVALU PETROLEUM COCOA BUTTERWHITE PETROLATUMJC SALES490af001-c78c-e2d2-e063-6394a90abdb02026-01-01WarningsExact identifier
unii: 4T6H12BN9U

Reported adverse events (FAERS/openFDA)#

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