WITCH HAZEL READYINCASE- witch hazel liquid

Witch Hazel by

Drug Labeling and Warnings

Witch Hazel by is a Otc medication manufactured, distributed, or labeled by P & L Development, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Witch hazel 86%

Purpose

Astringent

Uses

• for relief of minor skin irritations due to:
  • insect bites
  • minor cuts
  • minor scrapes

Warnings

• for external use only
• avoid swallowing

When using this product

• avoid contact with the eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

condition worsens or symptoms persist for more than 7 days.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

apply to the affected area as often as necessary.

Other information

• keep tightly closed
• store at room temperature

Inactive ingredient

alcohol 14% by volume

Principal Display Panel

Distilled extract of

Witch Hazel

Astringent

alcohol 14% by volume

Manufactured by:

PL Developments

1874 Hwy 72 W

Clinton, SC 29325

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND OR UNDER CAP IS BROKEN OR MISSING.

FL OZ(mL

Package Label

ReadyInCase Witch Hazel Liquid

INGREDIENTS AND APPEARANCE

WITCH HAZEL  READYINCASE
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49580-0390
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	86 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49580-0390-6	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/31/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part347	08/31/2014

Labeler - P & L Development, LLC (101896231)