OTC - ACTIVE INGREDIENT SECTION
sodium chloride
REAL SUMMER
- Manufacturer
- Kayone
- Effective date
- 2014-12-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:41:04
Label at a glance#
ProductREAL SUMMER
Active ingredientSODIUM CHLORIDE
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
iron powder, active carbon, resin vermiculite, salty water
OTC - PURPOSE SECTION
insect bite
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
keep out of reach of the children
INDICATIONS & USAGE SECTION
When pasting on the mosquito, red ant or other inset bite area, pure mild fever soothes itching, and furthermore soothes festered skin.It can be used for men and women of all ages without adverse effects.Pucca is a character loved by people all around the world, which gives cute and refined image to both infants and adults.
WARNINGS SECTION
Be careful for children not to put it to the mouse. Stop using if there is any problem in the use of the product.Keep it in a cool area without direct light.Store it with sealing after the use. Be careful that if attachment and detachment are repeated, its adhesiveness may decrease.
DOSAGE & ADMINISTRATION SECTION
for external use only
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69449-1001-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-e2b2-f424-e053-dadaa90a57ce | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69449-1001-1 | REAL SUMMER | 12 g in 1 PATCH | PATCH | 12 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69449-1001 | REAL SUMMER (SODIUM CHLORIDE) PATCH [KAYONE ] | 1 | Legacy NDC, 1 package rows | 20141214_a040d98f-ab5a-4a37-badc-59c96d32a306.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| SODIUM CHLORIDE | ACTIVE INGREDIENT | 451W47IQ8X | 1 | |
| CHLORIDE ION | ACTIVE MOIETY | Q32ZN48698 | 1 | |
| CARBON DIOXIDE | INACTIVE INGREDIENT | 142M471B3J | 1 | |
| IRON | INACTIVE INGREDIENT | E1UOL152H7 | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- REAL SUMMER
- SODIUM CHLORIDE
- CHLORIDE ION
- WATER
- IRON
- CARBON DIOXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69449-1001 | 69449-1001-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
| WATER | 059QF0KO0R | IACT |
| IRON | E1UOL152H7 | IACT |
| CARBON DIOXIDE | 142M471B3J | IACT |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| CARBON DIOXIDE | CARBON DIOXIDE | 142M471B3J | INJECTION / INTRAVENOUS | ADJ PH | ||
| IRON | IRON | E1UOL152H7 | TABLET, EXTENDED RELEASE / ORAL | 5 mg |
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 |
|---|---|---|---|---|---|---|
| 1ea4d8e4-9c9d-411c-b543-c9cb1d9ea0d2 | a040d98f-ab5a-4a37-badc-59c96d32a306 | 2014-12-08 | Warnings | 1ea4d8e4-9c9d-411c-b543-c9cb1d9ea0d2 a040d98f-ab5a-4a37-badc-59c96d32a306 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.