Naturasil
- Manufacturer
- Nature's Innovation, Inc.
- Effective date
- 2012-02-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:49:42
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
DrugFacts
Active Ingredients:
Natrum Muriaticum 6X HPUS
DESCRIPTION SECTION
The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.
OTC - PURPOSE SECTION
Purpose
Eczema Symptom ReliefINDICATIONS & USAGE SECTION
Uses: Symptomatic treatment of eczema.
WARNINGS SECTION
Warnings: For external use only.
OTC - ASK DOCTOR SECTION
Ask a doctor before use if pregnant or nursing.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
OTC - DO NOT USE SECTION
Do not use if tamper evident seal is broken.
OTHER SAFETY INFORMATION
In case on ingestion call Poison Control Center hotline immediately at 1-800-222-1222.
DOSAGE & ADMINISTRATION SECTION
Directions: Apply a few drops of product to the affected area 2-3 times per day, until the eczema symptoms have cleared. It can take from several days to weeks to heal the eczema. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Borage Seed Oil, Carrot Seed Oil, Chamomile Flower Oil, Helicrysum Flower Oil, Jojoba Seed Oil, Lavender Oil, Melaleuca Alternifolia Leaf Oil, Rose Hip Seed Oil.
OTC - QUESTIONS SECTION
Questions? Comments?
www.naturasil.com 1-866-371-2499
Mfd. by: Nature's Innovation, Inc.
2723 Brickton North Dr., Buford, GA 30518
Not tested on animals.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 10893-150-10 | 2020-02-04 | C162847 | 48780-1 | 9d75b9d0-b383-f424-e053-dadaa90a57ce | Eczema Label |
| 10893-150-15 | 2020-02-04 | C162847 | 48780-1 | 9d75b9d0-b383-f424-e053-dadaa90a57ce | Eczema Label |
| 10893-150-10 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-b383-f424-e053-dadaa90a57ce | Eczema Label |
| 10893-150-15 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-b383-f424-e053-dadaa90a57ce | Eczema Label |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| SODIUM CHLORIDE | ACTIVE INGREDIENT | 451W47IQ8X | 3 | |
| SODIUM | ACTIVE MOIETY | 9NEZ333N27 | 3 | |
| BORAGE OIL | INACTIVE INGREDIENT | F8XAG1755S | 3 | |
| CARROT SEED OIL | INACTIVE INGREDIENT | 595AO13F11 | 3 | |
| CHAMOMILE FLOWER OIL | INACTIVE INGREDIENT | 60F80Z61A9 | 3 | |
| HELICHRYSUM ITALICUM FLOWER OIL | INACTIVE INGREDIENT | O97ZV7726K | 3 | |
| JOJOBA OIL | INACTIVE INGREDIENT | 724GKU717M | 3 | |
| LAVENDER OIL | INACTIVE INGREDIENT | ZBP1YXW0H8 | 3 | |
| ROSA RUBIGINOSA SEED OIL | INACTIVE INGREDIENT | 8M1P49MWAP | 3 | |
| TEA TREE OIL | INACTIVE INGREDIENT | VIF565UC2G | 3 |
Products#
Every source-derived product name is available through these pages.
- Naturasil Eczema
- Natrum Muriaticum
- SODIUM CHLORIDE
- SODIUM
- BORAGE OIL
- CARROT SEED OIL
- CHAMOMILE FLOWER OIL
- HELICHRYSUM ITALICUM FLOWER OIL
- JOJOBA OIL
- LAVENDER OIL
- TEA TREE OIL
- ROSA RUBIGINOSA SEED OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10893-150 | 10893-150-10, 10893-150-15 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
| BORAGE OIL | F8XAG1755S | IACT |
| CARROT SEED OIL | 595AO13F11 | IACT |
| CHAMOMILE FLOWER OIL | 60F80Z61A9 | IACT |
| HELICHRYSUM ITALICUM FLOWER OIL | O97ZV7726K | IACT |
| JOJOBA OIL | 724GKU717M | IACT |
| LAVENDER OIL | ZBP1YXW0H8 | IACT |
| TEA TREE OIL | VIF565UC2G | IACT |
| ROSA RUBIGINOSA SEED OIL | 8M1P49MWAP | 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 |
|---|---|---|---|---|---|---|
| LAVENDER OIL | LAVENDER OIL | ZBP1YXW0H8 | INHALANT / NASAL | NA | ||
| LAVENDER OIL | LAVENDER OIL | ZBP1YXW0H8 | GEL / TOPICAL | 0.1 %w/w |
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 |
|---|---|---|---|---|---|---|
| fab0ab29-1f86-495f-829e-385594f5352e | 5c17f913-bb5c-4b91-bae8-2f7bbb946b72 | 2012-02-02 | Warnings | fab0ab29-1f86-495f-829e-385594f5352e 5c17f913-bb5c-4b91-bae8-2f7bbb946b72 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.


