Indications and uses
Sanitizer to help reduce bacteria on skin. For use when soap and water not available.
Swedish Dream Sea Salt Hand Sanitizer
- Manufacturer
- Kala Corporation
- Effective date
- 2022-01-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:46:47
Label at a glance#
ProductSwedish Dream Sea Salt Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections
Dosage and administration
Apply on hands and rub until dry.
Label contents#
Full prescribing information#
Active Ingredient
Ethyl Alcohol 65%
Purpose
Antiseptic
Uses
Sanitizer to help reduce bacteria on skin. For use when soap and water not available.
Warnings
For external use only. Keep away from heat or flame.
When using this product
Keep out of eyes. In case of contact, flush thoroughly with water.
Keep out of reach of children
If swallowed get medical help or contact a poison control center right away.
Directions:
Apply on hands and rub until dry.
Other Information
Store between 15-30C(59-86F) - Avoid freezing and excess heat over 40C(104F)
Inactive Ingredients
Deionized Water, Glycerine, Sea Salt Essence (Fragrance Oil)
Sea Salt Hand Sanitizer Label
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 79655-606-01 | 2023-07-28 | C162847 | 48780-1 | 0191ceaa-69fd-198a-e063-dbdaa90aec3e | Swedish Dream® Sea Salt Hand Sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79655-606-01 | Swedish Dream Sea Salt Hand Sanitizer | 59 mL in 1 BOTTLE, SPRAY | LIQUID | 59 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Swedish Dream Sea Salt Hand Sanitizer
- Ethyl Alcohol Formulation
- LINALOOL, (+/-)-
- WATER
- ALCOHOL
- PHENYLETHYL ALCOHOL
- 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL
- LINALYL ACETATE
- ABIES SIBIRICA LEAF OIL
- .ALPHA.-AMYLCINNAMALDEHYDE DIMETHYL ACETAL
- METHYL BENZODIOXEPINONE
- 8-(N-INDOLYL)-2,6-DIMETHYL-7-OCTEN-2-OL
- HYDROXYCITRONELLAL
- CYCLAMEN ALDEHYDE
- 2,6,10-TRIMETHYL-9-UNDECENAL
- 2-METHYLUNDECANAL
- 2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OL
- GLYCERIN
- ETHYLENE BRASSYLATE
- .ALPHA.-TERPINEOL
- BENZYL SALICYLATE
- ISOAMYL SALICYLATE
- 3-HEXENYL SALICYLATE, CIS-
- METHYL 2-NONYNOATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 79655-606 | 79655-606-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| d578f0b0-5e5d-1ef2-e053-2995a90ae7c1 | aaa4fdad-2f07-dd39-e053-2a95a90a85bb | 2022-01-13 | Warnings | d578f0b0-5e5d-1ef2-e053-2995a90ae7c1 aaa4fdad-2f07-dd39-e053-2a95a90a85bb |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.