RUMEX CRISPUS- yellow dock granule
Seroyal USA

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.

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RUMEX CRISPUS

Active Ingredient

RUMEX CRISPUS 200K GR

RUMEX CRISPUS 30CH GR

RUMEX CRISPUS 30K GR

Indications

For the temporary relief of coughs and gastric
discomforts

Warning:
If pregnant or breastfeeding, ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Inactive Ingredients
Lactose,
sucrose.

Directions
Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
Children: Take three granules and follow adult directions.

QUESTIONS? 1-888-737-6925.

Indications

For the temporary relief of coughs and gastric
discomforts

Directions
Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
Children: Take three granules and follow adult directions.

62106-8802

UNDA
Do not use if label perforation is broken
Homeopathic Remedy
NDC : 62106-8802-4
RUMEX CRISPUS
Yellow dock
140 granules
Indications

For the temporary relief of coughs and gastric
discomforts

RUMEX CRISPUS
yellow dock granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62106-8802
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C)	RUMEX CRISPUS ROOT	1 [hp_X]

Ingredient Name	Strength
Inactive Ingredients
LACTOSE (UNII: J2B2A4N98G)
SUCROSE (UNII: C151H8M554)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62106-8802-4	10 in 1 CARTON	04/30/2015	05/31/2022
1		140 in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		04/30/2015	05/31/2022

Labeler - Seroyal USA (018361118)

Name	Address	ID/FEI	Business Operations
Establishment
SAN’UP		401010287	manufacture(62106-8802)

Revised: 10/2023

Document Id: 06e8042e-30ab-163b-e063-6294a90a74f3

Set id: 14f4b9f2-1169-07b3-e054-00144ff8d46c

Version: 4

Effective Time: 20231004

Seroyal USA