Indications and uses
helps prevent and temporarily protects chafed, chapped or cracked skin helps protect from the drying effects of wind and cold weather
H-E-B DAILY MOISTURIZING LOTION
- Manufacturer
- H.E.B | Fruit of the Earth, Inc.
- Effective date
- 2020-03-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:39:15
Label at a glance#
ProductH.E.B
Active ingredientDIMETHICONE
Label structure13 sections
Dosage and administration
apply as needed to hands or body when skin feels dry or irritated
Contacts and useful links#
Label contents#
Full prescribing information#
Active Ingredients
Dimethicone 1.2%
Purpose
Sunscreen
Uses
- helps prevent and temporarily protects chafed, chapped or cracked skin
- helps protect from the drying effects of wind and cold weather
Warnings
For external use only
OTC - DO NOT USE SECTION
Do not use on • deep or puncture wounds • animal bites • serious burns
OTC - WHEN USING SECTION
When using this product • do not get into eyes
OTC - ASK DOCTOR SECTION
Stop use and ask a doctor if • condition worsens • symptoms last more than seven days or clear up and occur again within a few days
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center right away.
Directions
- apply as needed to hands or body when skin feels dry or irritated
Other Information
- may stain some fabrics
Inactive Ingredient(s)
water, glycerin, distearyldimonium chloride, petrolatum, isopropyl palmitate, cetyl alcohol, avena sativea (oat) kernel flour, benzyl alcohol, sodium chloride.
Questions?
Call toll free 1-800-527-7731
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
H-E-B DAILY MOISTURIZING LOTION
18 FL OZ (532mL)
NDC 37808-927-43
Products#
Every source-derived product name is available through these pages.
- H.E.B
- DAILY MOISTURIZING
- DIMETHICONE
- WATER
- GLYCERIN
- DISTEARYLDIMONIUM CHLORIDE
- PETROLATUM
- ISOPROPYL PALMITATE
- CETYL ALCOHOL
- OATMEAL
- BENZYL ALCOHOL
- MAGNESIUM ALUMINUM SILICATE
- SODIUM CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 37808-927 | 37808-927-43 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIMETHICONE | 92RU3N3Y1O | ACTIB |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| DISTEARYLDIMONIUM CHLORIDE | OM9573ZX3X | IACT |
| PETROLATUM | 4T6H12BN9U | IACT |
| ISOPROPYL PALMITATE | 8CRQ2TH63M | IACT |
| CETYL ALCOHOL | 936JST6JCN | IACT |
| OATMEAL | 8PI54V663Y | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
| MAGNESIUM ALUMINUM SILICATE | 6M3P64V0NC | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| c718f93e-3cc9-6045-e053-2a95a90a8bb7 | 17eec39e-7dd6-4cee-9d43-4d9c6a434407 | 2023-02-16 | Warnings | 17eec39e-7dd6-4cee-9d43-4d9c6a434407 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.