BACH FEAR NO MORE BRAVERY KIT- aspen, cherry plum, rock rose kit

Bach Fear No More Bravery Kit by

Drug Labeling and Warnings

Bach Fear No More Bravery Kit by is a Homeopathic medication manufactured, distributed, or labeled by Nelson Bach USA Limited, A. Nelson & Co. Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient (Each 5X HPUS)............... Purpose

Bottle 1: Aspen...............................................Feel secure

Bottle 2: Cherry Plum.....................................Be in control

Bottle 3: Rock Rose.......................................Have courage

'HPUS' indicates ingredients are in the official Homeopathic Pharmacopoeia of the United States

Use

For relief of naturally occuring simple nervous tension

Warnings

Consult a doctor if symptoms last for more than 7 days or worsen.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

Directions

■ single remedies: take 2 drops directly on the tongue or add to a beverage & sip. Repeat as needed throughout the day.
■ children under 2: ask a doctor before use

Other information

■ store below 77ºF (25ºC)
■ do not use if tamper evident seal around bottle neck is missing or broken

Inactive ingredients

glycerin [vegetable], purified water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BACH FEAR NO MORE BRAVERY KIT 
aspen, cherry plum, rock rose kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57687-313

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57687-313-30	1 in 1 CARTON	11/01/2023

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE, DROPPER	10 mL
Part 2	1 BOTTLE, DROPPER	10 mL
Part 3	1 BOTTLE, DROPPER	10 mL

Part 1 of 3

BACH ORIGINAL FLOWER REMEDIES ROCK ROSE 
helianthemum nummularium solution

Product Information
Item Code (Source)	NDC: 57687-225
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (HELIANTHEMUM NUMMULARIUM FLOWER - UNII:51BRR32WPP)	HELIANTHEMUM NUMMULARIUM FLOWER	5 [hp_X]  in 0.095 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57687-225-10	1 in 1 CARTON
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/01/2023

Part 2 of 3

BACH ORIGINAL FLOWER REMEDIES ASPEN 
populus tremula solution

Product Information
Item Code (Source)	NDC: 57687-201
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POPULUS TREMULA FLOWERING TOP (UNII: 5Q01F7TPJJ) (POPULUS TREMULA FLOWERING TOP - UNII:5Q01F7TPJJ)	POPULUS TREMULA FLOWERING TOP	5 [hp_X]  in 0.095 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57687-201-10	1 in 1 CARTON
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/01/2023

Part 3 of 3

BACH ORIGINAL FLOWER REMEDIES CHERRY PLUM 
prunus cerasifera solution

Product Information
Item Code (Source)	NDC: 57687-205
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (PRUNUS CERASIFERA FLOWER - UNII:0KD7R09EAS)	PRUNUS CERASIFERA FLOWER	5 [hp_X]  in 0.095 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57687-205-10	1 in 1 CARTON
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/01/2023

Labeler - Nelson Bach USA Limited (877720193)

Registrant - A. Nelson & Co. Limited (224171234)

Establishment
Name	Address	ID/FEI	Business Operations
A. Nelson & Co. Limited		221471234	manufacture(57687-313)