Mentholatum Natural Ice

Product NDC
10742-3004
11-digit product format
107423004
Labeler code
10742
Product ID
10742-3004_4dbf3ecb-629f-bbfc-e063-6294a90ad6a0
Type
HUMAN OTC DRUG
Nonproprietary name
dimethicone, octinoxate, octisalate
Dosage form
OINTMENT
Route
TOPICAL
Labeler
The Mentholatum Company
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
1999-01-19
Substance
DIMETHICONE; OCTINOXATE; OCTISALATE
Active strength
10; 75; 50 mg/g; mg/g; mg/g
Pharmacologic classes
Skin Barrier Activity [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage10742-300410742-3004-1DDiscontinued by firm2026-08-17
excluded packagepackage10742-300410742-3004-9DDiscontinued by firm2026-08-17

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Package NDC, Snapshot table
Captured / source datePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-0510742-3004-1d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0510742-3004-9d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-2610742-3004-1f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2610742-3004-9f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-3110742-3004-12ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3110742-3004-92ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-2810742-3004-1a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2810742-3004-9a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-2110742-3004-1cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2110742-3004-9cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-1010742-3004-1cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1010742-3004-9cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-3110742-3004-1302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-3110742-3004-9302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-2010742-3004-1ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-2010742-3004-9ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-1010742-3004-10efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-1010742-3004-90efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-0810742-3004-1ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-0810742-3004-9ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-0310742-3004-1367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-0310742-3004-9367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-0910742-3004-1557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-0910742-3004-9557ba5c1ecfa…9c80585c8c6e…

Additional Listing Data#

Finished product
Yes
Brand name base
Mentholatum Natural Ice
Brand name suffix
Original
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTISALATE10 mg/g
DIMETHICONE75 mg/g
OCTINOXATE50 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4X49Y0596WInternal UNII lookup
92RU3N3Y1OInternal UNII lookup
4Y5P7MUD51Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
29220eaa-87cb-4ebe-87db-d36288b3a9e4Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10742-3004-1Mentholatum Natural IceOriginal4.5 g in 1 TUBEOINTMENT4.513
10742-3004-1Mentholatum Natural IceOriginal1 in 1 BLISTER PACKOINTMENT113
10742-3004-2Mentholatum Natural IceOriginal4.2 g in 1 TUBEOINTMENT4.213
10742-3004-2Mentholatum Natural IceOriginal1 in 1 BLISTER PACKOINTMENT113
10742-3004-3Mentholatum Natural IceOriginal4.5 g in 1 TUBEOINTMENT4.513
10742-3004-3Mentholatum Natural IceOriginal1 in 1 BLISTER PACKOINTMENT113
10742-3004-4Mentholatum Natural IceOriginal4.5 g in 1 TUBEOINTMENT4.513
10742-3004-8Mentholatum Natural IceOriginal4.2 g in 1 TUBEOINTMENT4.213
10742-3004-9Mentholatum Natural IceOriginal4.5 g in 1 TUBEOINTMENT4.513

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DIMETHICONEACTIVE INGREDIENT92RU3N3Y1OMENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD51MENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
OCTISALATEACTIVE INGREDIENT4X49Y0596WMENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
DIMETHICONEACTIVE MOIETY92RU3N3Y1OMENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
OCTINOXATEACTIVE MOIETY4Y5P7MUD51MENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
OCTISALATEACTIVE MOIETY4X49Y0596WMENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
CERESININACTIVE INGREDIENTQ1LS2UJO3AMENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
LANOLININACTIVE INGREDIENT7EV65EAW6HMENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
MENTHOLINACTIVE INGREDIENTL7T10EIP3AMENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
MINERAL OILINACTIVE INGREDIENTT5L8T28FGPMENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2
PETROLATUMINACTIVE INGREDIENT4T6H12BN9UMENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10742-3004MENTHOLATUM NATURAL ICE ORIGINAL (DIMETHICONE, OCTINOXATE, OCTISALATE) OINTMENT [THE MENTHOLATUM COMPANY]12Current NDC, Legacy NDC, 9 package rows20241215_29220eaa-87cb-4ebe-87db-d36288b3a9e4.zip

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 361 · 7,202 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ISNTREE HYALURONIC ACID SENSITIVE SUNSCREENZINC OXIDEISNTREE Inc.58e38665-0bca-fb02-e063-6394a90ad62a2026-08-13WarningsExact identifier
application number: M020
Neutrogena Ultra Sheer Daily Face Sunscreen Broad Spectrum SPF 70AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATEKenvue Brands LLC58d3d390-8b88-a6fe-e063-6394a90a9bf82026-08-12WarningsExact identifier
application number: M020
Neutrogena Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATEKenvue Brands LLC58d7a3e3-b7df-43ce-e063-6294a90a729c2026-08-12WarningsExact identifier
application number: M020
Elta MD Skincare UV Stick Broad Spectrum SPF50ZINC OXIDECP Skin Health Group, Inc58dd81db-46d4-d763-e063-6394a90abb0b2026-08-12WarningsExact identifier
application number: M020
UV Skin Recovery SPF 50 Red CorrectingZINC OXIDECP Skin Health Group, Inc.26e63890-d1af-d171-e063-6394a90af8282026-08-12WarningsExact identifier
application number: M020
UV Skin Recovery SPF 50ZINC OXIDECP Skin Health Group, Inc.26d2683f-cfd5-50fd-e063-6394a90a75762026-08-12WarningsExact identifier
application number: M020
doTERRA Sun BodyMINERAL SUNSCREENdoTERRA International, LLC58dcc56f-f093-469c-e063-6394a90a60882026-08-12WarningsExact identifier
application number: M020
Colorescience Total Protection Body Shield GlowZINC OXIDEColorescience52e1d987-a4f8-195e-e063-6294a90a56292026-08-11WarningsExact identifier
application number: M020
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30DR. SAMRAO'S OFFICE58b2ca35-11ed-d848-e063-6294a90a5b372026-08-11WarningsExact identifier
application number: M020
Ciele Tint and ProtectZINC OXIDECiele0162d9c9-07fa-9210-e063-6294a90aa6872026-08-11WarningsExact identifier
application number: M020
NeoStrata Skin Active Matrix Support SPF 30AVOBENZONE, OCTINOXATE, AND OCTISALATENeoStrata Company Inc.8e4b9c08-b906-4c5f-a243-55838ae28b902026-08-10WarningsExact identifier
application number: M020
HEADHUNTER SURF SCREEN SPF 50 SUNSCREENZINC OXIDE,TITANIUM DIOXIDEGuangzhou Tata Biotechnology Co., Ltd.4339df13-77d3-31a1-e063-6394a90a52082026-08-10WarningsExact identifier
application number: M020
Sunscreen for Kids SPF 50AVOBENZONE, HOMOSALATE, OCTISALATEThe Kroger Co.1c7cd904-ffff-48aa-91bd-cc978946b36a2026-08-10Warnings, Adverse reactionsExact identifier
application number: M020
Sport Sunscreen SPF 50AVOBENZONE, HOMOSALATE, OCTISALATEThe Kroger Co.22aa46af-5d0f-4256-8f45-be06f66275612026-08-10WarningsExact identifier
application number: M020
Colorescience Total Protection No Show Mineral Body ShieldZINC OXIDEColorescience52e1f59e-63cb-7480-e063-6394a90ad7c52026-08-10WarningsExact identifier
application number: M020
Journee Firm Riche Broad Spectrum Sunscreen SPF 30TITANIUM DIOXIDE AND ZINC OXIDEMerz North America, Inc.d4d4bfcf-3674-4847-8ad8-1716a8e821ae2026-08-10WarningsExact identifier
application number: M020
ULTRA VIOLETTE Unblock Screen SPF 50 SunscreenBEMOTRIZINOL, OCTOCRYLENE, ZINC OXIDEGrace and Fire USA Inc.56ad0dce-410e-9d78-e063-6294a90a1c3e2026-08-09WarningsExact identifier
application number: M020
ORLASKIN SPF50 Antioxidant SoothingComplex SunscreenETHYLHEXYL METHOXYCINNAMATE ETHYLHEXYL SALICYLATE BUTYL METHOXYDIBENZOYLMETHANE ZINC OXIDE BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINEGuangzhou Yapheon Health Industry Co., Ltd.552a36ed-7a66-4048-e063-6394a90a09bc2026-08-08WarningsExact identifier
application number: M020
lip balm SPF15( 2533) 01AVOBENZONE,HOMOSALATE,OCTOCRYLENE,OCTISALATECosmuses Cosmetics (Ningbo) Co., Ltd.5870aa44-1375-cdc5-e063-6394a90af4a52026-08-07WarningsExact identifier
application number: M020
lip balm SPF15( Zinc oxide) 01ZINC OXIDECosmuses Cosmetics (Ningbo) Co., Ltd.5871ab1d-cf07-d737-e063-6394a90a58fe2026-08-07WarningsExact identifier
application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10742-3004-1107423004014.5 g in 1 TUBE4.5 gHistorical
10742-3004-2107423004021 TUBE in 1 BLISTER PACK (10742-3004-2) / 4.2 g in 1 TUBE1 tube2019-04-020000-00-00NoNoCurrent
10742-3004-3107423004031 TUBE in 1 BLISTER PACK (10742-3004-3) / 4.5 g in 1 TUBE1 tube1999-01-190000-00-00NoNoCurrent
10742-3004-4107423004044.5 g in 1 TUBE (10742-3004-4) 4.5 g1999-01-190000-00-00NoNoCurrent
10742-3004-8107423004084.2 g in 1 TUBE (10742-3004-8) 4.2 g2019-04-020000-00-00NoNoCurrent
10742-3004-9107423004094.5 g in 1 TUBE4.5 gHistorical