365 Everyday Value Arnica Gel
- Manufacturer
- WFM Private Label, LP
- Effective date
- 2023-07-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 15
- Source
- full-release
- Hydrated at
- 2026-06-01 02:21:46
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient †
Arnica montana 1X HPUS - 7%
The letters "HPUS" indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.
OTC - PURPOSE SECTION
Purpose*
Arnica montana 1X HPUS - 7% ... Trauma, bruises, stiffness, muscle soreness
INDICATIONS & USAGE SECTION
Uses*
For relief of muscle aches and stiffness due to:
- minor injuries
- strains
- falls and blows
- Reduces pain, swelling and discoloration from bruises
WARNINGS SECTION
For external use only
OTC - DO NOT USE SECTION
Do not use if you are allergic to Arnica montana or to any of this product's inactive ingredients.
OTC - WHEN USING SECTION
When using this product
- avoid contact with eyes, mucous membranes, wounds, damaged or irritated skin
- use only as directed
- dryness or irritation may occur
- do not tightly wrap or bandage the treated area
- do not apply heat or ice to the treated area immediately before or after use
OTC - ASK DOCTOR SECTION
Stop use and ask a doctor if
- condition persists for more than 3 days or worsens
- symptoms clear up and reoccur 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.
DOSAGE & ADMINISTRATION SECTION
Directions Apply a thin layer of Arnica Gel to affected area as soon as possible after minor injury. Repeat 3 times a day or as needed. If heat or ice is applied, wait 5 minutes before applying Arnica Gel.
SPL UNCLASSIFIED SECTION
Other information
- do not store above 86° F (30° C)
- do not use if glue carton end flaps are open or if tube seal is broken
INACTIVE INGREDIENT SECTION
Inactive ingredients alcohol, carbomer, purified water, sodium hydroxide
SPL UNCLASSIFIED SECTION
Pain relief of sore muscles, swelling, stiffness & bruising*
Homeopathic Medicine
NET WT 2.6 OZ (75g)
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
†C,K,CK, and X are homeopathic dilutions: see
www.theAAHP.org for details
OTC - QUESTIONS SECTION
Questions or comments?
1-844-WFM-TALK (1-844-936-8255)
Distributed by:
Whole Foods Market
Austin, TX 78703
© 2020 WHOLE FOODS MARKET IP, LP
MADE IN FRANCE
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 42681-0512-5 | 365 Everyday Value Arnica | 1 in 1 BOX | GEL | 1 | 15 | |
| 42681-0512-6 | 365 Everyday Value Arnica | 1 in 1 BOX | GEL | 1 | 15 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 42681-0512 | 365 EVERYDAY VALUE ARNICA (ARNICA MONTANA) GEL [WFM PRIVATE LABEL, LP] | 15 | Current NDC, Legacy NDC, 2 package rows | 20230719_43546269-d873-45d6-863f-e794446ef388.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ARNICA MONTANA | ACTIVE INGREDIENT | O80TY208ZW | 7 | |
| ARNICA MONTANA | ACTIVE MOIETY | O80TY208ZW | 7 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 7 | |
| CARBOMER HOMOPOLYMER TYPE C | INACTIVE INGREDIENT | 4Q93RCW27E | 7 | |
| DIMETHICONE | INACTIVE INGREDIENT | 92RU3N3Y1O | 7 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | 7 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 7 |
Products#
Every source-derived product name is available through these pages.
- 365 Everyday Value Arnica
- ARNICA MONTANA
- WATER
- ALCOHOL
- CARBOMER HOMOPOLYMER TYPE C
- SODIUM HYDROXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 42681-0512 | 42681-0512-5, 42681-0512-6 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| CARBOMER HOMOPOLYMER TYPE C | 4Q93RCW27E | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| ARNICA MONTANA | O80TY208ZW | ACTIB |
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 |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | GEL / TOPICAL | 70 mg | ||
| CARBOMER HOMOPOLYMER TYPE C | CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | GEL / TOPICAL | 85 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| CARBOMER HOMOPOLYMER TYPE C | CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | GEL / TOPICAL | 85 mg | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | GEL / TOPICAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | GEL / TOPICAL | 70 mg | ||
| CARBOMER HOMOPOLYMER TYPE C | CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) | 4Q93RCW27E | GEL / TOPICAL | 85 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 |
|---|---|---|---|---|---|---|
| 365 Everyday Value Arnica | ARNICA MONTANA | WFM Private Label, LP | 43546269-d873-45d6-863f-e794446ef388 | 2023-07-18 | Warnings | 42681-0512-6 42681-0512-5 42681-0512 42681051206 42681051205 00c741d4-f9a5-b286-e063-6394a90adb2c 43546269-d873-45d6-863f-e794446ef388 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.




