Witch Hazel by H-E-B / Vi-Jon WITCH HAZEL liquid

Witch Hazel by

Drug Labeling and Warnings

Witch Hazel by is a Otc medication manufactured, distributed, or labeled by H-E-B, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Witch Hazel 86%

Purpose

Astringent

Use

REMOVE STICKER ON PUMP PRIOR TO USE.  (FOR PUMP BOTTLES)

for relief of minor skin irritations due to:

• insect bites
• minor cuts
• minor scrapes

Warnings

For external use only

When using this product

avoid contact with the eyes

Stop use and ask a doctor if

• condition worsens or symptoms persist for more than 7 days

Keep out of reach of children.

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

Directions

apply as often as needed

For Pump

remove sticker prior to use.  Pump onto a clean pad and apply as often as needed.

Inactive ingredient

alcohol 14% by volume

adverse reaction

MADE WITH PRIDE  & CARE FOR

H-E-B, SAN ANTONIO, TX 78204

822.001/822AA

principal display panel

PUSH PUMP

H-E-B

Witch Hazel U.S.P.

Astringent

• Cleans & Refreshes
• For Relief of Minor Skin Irritations due to Insects Bites, Minor Cuts and Minor Scrapes

8 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

WITCH HAZEL 
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-822
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	979 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-822-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/18/2015
2	NDC: 37808-822-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/18/2015
3	NDC: 37808-822-99	236 mL in 1 BOTTLE, PUMP; Type 1: Convenience Kit of Co-Package	06/18/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	06/18/2015

Labeler - H-E-B (007924756)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(37808-822)