Bach Letting Go

Manufacturer
Nelson Bach USA Ltd | A. Nelson & Co. Ltd.
Effective date
2026-09-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-10-13 04:02:22

Label at a glance#

ProductBach Letting Go
Active ingredientULMUS PROCERA FLOWERING TWIG, AESCULUS CARNEA FLOWER, JUGLANS REGIA FLOWERING TOP
Label structure8 sections

Dosage and administration

Put 4 drops onto the tongue or into a drink, up to 4 times per day Children under 12: ask a doctor before use

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

(Each: equal parts 5X HPUS)

Elm (Ulmus procera)

Red Chestnut (Aesculus carnea)

Walnut (Juglans regia)

'HPUS' indicates the ingredient is in the official Homeopathic Pharmacopoiea of the United States

Purpose

OTC - PURPOSE SECTION

Elm - Be efficient

Red Chestnut - Peace of mind

Walnut - Adapt to change

Use

INDICATIONS & USAGE SECTION

For relief of naturally occuring simple nervous tension

Warnings

WARNINGS SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put 4 drops onto the tongue or into a drink, up to 4 times per day
  • Children under 12: ask a doctor before use

Other information

OTHER SAFETY INFORMATION

  • Do not use if tamper evident seal around bottle neck is missing or broken
  • Store below 77°F (25°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

grape alcohol (27% v/v)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Letting Go CartonLetting Go CartonBach Original Flower Remedies

Letting Go

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix4200156Bach Letting Go.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57687-35257687-352-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.