FDA.reportPublic FDA data

Harmon Face Values All-Day Skin Relief Moisturizing Lotion

Manufacturer
HARMON STORES, INC.
Effective date
2024-10-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:51:45

Label at a glance#

ProductHarmon Face Values All-Day Skin Relief Moisturizing
Active ingredientDIMETHICONE
Label structure12 sections

Indications and uses

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

Dosage and administration

apply as needed to hands or body when skin feels dry or irritated

Storage and handling

• may stain some fabrics

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Dimethicone 1.2%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

• do not get into eyes

Do not use on

OTC - DO NOT USE SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • condition worsens
  • symptoms last more than seven 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 to hands or body when skin feels dry or irritated

Other Information

STORAGE AND HANDLING SECTION

• may stain some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, distearyldimonium chloride, petrolatum, isopropyl palmitate, cetyl alcohol, avena sativa (oat) kernel flour, benzyl alcohol, avena sativa (oat) kernel oil, steareth-20, avena sativa (oat) kernel extract, butyrospermum parkii (shea) butter, potassium sorbate, sodium chloride

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

42286E1F142286E1F1

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63940-08963940-089-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
SHEA BUTTERK49155WL9YIACT
DISTEARYLDIMONIUM CHLORIDEOM9573ZX3XIACT
OATMEAL8PI54V663YIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM CHLORIDE451W47IQ8XIACT
PETROLATUM4T6H12BN9UIACT
CETYL ALCOHOL936JST6JCNIACT
OAT KERNEL OIL3UVP41R77RIACT
STEARETH-20L0Q8IK9E08IACT
OATZ6J799EAJKIACT
BENZYL ALCOHOLLKG8494WBHIACT
DIMETHICONE92RU3N3Y1OACTIB

Source Document#

Source XML

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
2503274d-1f71-bc11-e063-6394a90ab47ff31f135b-d46a-1b9f-e053-2a95a90a889d2024-10-21WarningsExact identifier
spl id: 2503274d-1f71-bc11-e063-6394a90ab47f
spl set id: f31f135b-d46a-1b9f-e053-2a95a90a889d

Reported adverse events (FAERS/openFDA)#

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