Rapidol Arnica Gel (CMHP) Deactivated

Rapidol Arnica by

Drug Labeling and Warnings

Rapidol Arnica by is a Homeopathic medication manufactured, distributed, or labeled by Pharmadel LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RAPIDOL ARNICA- arnica montana gel 
Pharmadel LLC

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

----------

Rapidol Arnica Gel (CMHP) Deactivated

Drug Facts

Active ingredient & Purposes

• Active Ingredient **: Purposes*
• Arnica montana 1 X HPUS ........................................................: Muscle aches and pains, bruises, swelling from injuries

The letters “HPUS” indicate that the components in this product are officially included in the Homeopathic Pharmacopoeia of the United States.

Uses

Helps relieve muscle aches and pains, bruises and swelling from injuries.

Warnings

FOR EXTERNAL USE ONLY. Avoid contact with the eyes.

Do not use

• on wounds or damaged skin
• on a bandage tightly

Stop use and consult a doctor

• condition worsens
• symptoms persist for more than 7 days or occur again within a few days
• rash develops

if pregnant or breastfeeding,

consult a doctor before using this product.

KEEP OUT OF THE REACH OF CHILDREN.

If swallowed, get medical help or contact a Poison Center right away.

Directions

• adults and children 12 years of age and older: apply a generous amount to the affected area not more than 2 to 3 times daily.
• children under 12 years of age: consult a doctor

Other information

• store in a cool dry place
• do not use if foil seal under cap is torn, broken, or missing

Inactive ingredients

aloe vera leaf, capryloyl glycine, hexylene glycol, hydroxyethyl cellulose, phenoxyethanol, potassium sorbate, methyl salicylate, water.

Questions or comments?

1-866-359-3478 (M-F) 9AM to 5 PM EST or www.pharmadel.com

Distributed by:

PHARMADEL LLC. ®
New Castle, DE, 19720

*These “USES” claims have not been evaluated by the Food and Drug Administration (FDA). They are based upon traditional homeopathic practices.
**C, K, CK, and X are homeopathic dilutions.

Principal Display Panel

RAPIDOL ARNICA 
arnica montana gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55758-032
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA WHOLE - UNII:O80TY208ZW)	ARNICA MONTANA WHOLE	1 [hp_X]  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYL SALICYLATE (UNII: LAV5U5022Y)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55758-032-02	57 g in 1 TUBE; Type 0: Not a Combination Product	03/15/2022	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/30/2020	12/31/2022

Labeler - Pharmadel LLC (030129680)

Revised: 1/2023

Document Id: 04287686-ea02-4a56-e063-6394a90a54b5

34390-5

Set id: b2e911f9-254b-7ab1-e053-2a95a90a102c

Version: 5

Effective Time: 20230101