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Drug Facts

Manufacturer
L’Oreal USA Products Inc | L’Oreal USA, Inc.
Effective date
2026-09-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-22 03:02:07

Label at a glance#

ProductKIEHLS ULTRA MELTDOWN MENDING MEDICATED LIP PROTECTANT
Active ingredientDIMETHICONE
Label structure12 sections

Indications and uses

helps prevent, temporarily protects and helps relieve chapped or cracked lips helps prevent and protect from the drying effects of wind and cold weather

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Dimethicone 1.1%

Purpose

OTC - PURPOSE SECTION

Lip protectant

Uses

INDICATIONS & USAGE SECTION

  • helps prevent, temporarily protects and helps relieve chapped or cracked lips
  • helps prevent and protect from the drying effects of wind and cold weather

Warnings

WARNINGS SECTION

For external use only

Do not use on

OTC - DO NOT USE SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

OTC - WHEN USING SECTION

do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply as needed

Inactive ingredients

INACTIVE INGREDIENT SECTION

octyldodecanol, dicaprylyl ether, glycerin, ethylcellulose, water, propanediol, sucrose laurate, sucrose palmitate, propylene glycol, panthenol, capryloyl glycine, caprylyl glycol, carbomer, ceramide AP, ceramide EOP, ceramide NP, cholesterol, citric acid, ectoin, ethylhexyl palmitate, lactic acid, magnesium sulfate, palmitoyl tripeptide-1, phytosphingosine, pseudoalteromonas ferment extract, sodium hydroxide,
sodium lauroyl lactylate, sorbitan isostearate, tocopherol, tribehenin, triethyl citrate, xanthan gum, benzoic acid, salicylic acid

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-888-577-5226
Monday -Friday (9 a.m. - 5 p.m. EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cartoncartontubetube

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82046-84482046-844-01, 82046-844-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 33 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OACTIB
OCTYLDODECANOL461N1O614YIACT
DICAPRYLYL ETHER77JZM5516ZIACT
GLYCERINPDC6A3C0OXIACT
ETHYLCELLULOSE7Z8S9VYZ4BIACT
WATER059QF0KO0RIACT
PROPANEDIOL5965N8W85TIACT
SUCROSE LAURATE05Q7CD0E49IACT
SUCROSE PALMITATE3OSQ643ZK5IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PANTHENOLWV9CM0O67ZIACT
CAPRYLOYL GLYCINE8TY5YO42NJIACT
CAPRYLYL GLYCOL00YIU5438UIACT
CARBOMER0A5MM307FCIACT
CERAMIDE APF1X8L2B00JIACT
CERAMIDE NP4370DF050BIACT
CHOLESTEROL97C5T2UQ7JIACT
CITRIC ACID2968PHW8QPIACT
ECTOIN7GXZ3858RYIACT
ETHYLHEXYL PALMITATE2865993309IACT
LACTIC ACID33X04XA5ATIACT
MAGNESIUM SULFATEDE08037SABIACT
PALMITOYL TRIPEPTIDE-1RV743D216MIACT
PHYTOSPHINGOSINEGIN46U9Q2QIACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM LAUROYL LACTYLATE7243K85WFOIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
TOCOPHEROLR0ZB2556P8IACT
TRIBEHENIN8OC9U7TQZ0IACT
TRIETHYL CITRATE8Z96QXD6UMIACT
XANTHAN GUMTTV12P4NEEIACT
BENZOIC ACID8SKN0B0MIMIACT
SALICYLIC ACIDO414PZ4LPZIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-06-01daily-update2026-06-04 05:10:19

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
5331ad70-94dd-d70b-e063-6394a90a4220c6bec79f-09cb-4836-9152-2ccdb2cde01d2026-06-01WarningsExact identifier
spl set id: c6bec79f-09cb-4836-9152-2ccdb2cde01d

Reported adverse events (FAERS/openFDA)#

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