WOUND CARE- wound care ointment ointment
Hunan Xiong Shi Pharmaceutical Co., Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredients

Zinc Oxide--0.5%

Inactive Ingredients

Bees Wax, Linoleic Acid, Propolis, Sesame Oil and a combination of all-natural Chinese Herbs

Keep out of reach of children.

If swallowed, call poison control or seek medical help.

Consulting a doctor before using

on deep or puncture wounds, animal bites or serious burns.

Stop use and ask a doctor

if your condition worsens, does not improve, persists for more than 7 days, or occurs again after a few days.

Purpose

Skin Protectant

Other information

Store at room temperature. may stain fabrics

Directions

Wash with mild skin cleanser. Pat dry or allow to air dry. Apply an ample amount of ointment over affected skin. Cover with a clean bandage. Repeat procedure every 12 hours until skin improves or as directed by a doctor.

Dosage & administration

When using this product

Do not get into eyes

Warnings

For external use only,

When using this product do not get into eyes

Label

WOUND CARE
wound care ointment ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73252-133
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.5 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
LINOLEIC ACID (UNII: 9KJL21T0QJ)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
SESAME OIL (UNII: QX10HYY4QV)
YELLOW WAX (UNII: 2ZA36H0S2V)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:73252-133-02	25 g in 1 BOTTLE; Type 0: Not a Combination Product	05/07/2019
2	NDC:73252-133-03	50 g in 1 BOTTLE; Type 0: Not a Combination Product	05/07/2019
3	NDC:73252-133-04	100 g in 1 BOTTLE; Type 0: Not a Combination Product	05/07/2019
4	NDC:73252-133-01	15 g in 1 BOTTLE; Type 0: Not a Combination Product	05/07/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	05/07/2019

Labeler - Hunan Xiong Shi Pharmaceutical Co., Ltd (554497403)

Registrant - Hunan Xiong Shi Pharmaceutical Co., Ltd (554497403)

Name	Address	ID/FEI	Business Operations
Establishment
Hunan Xiong Shi Pharmaceutical Co., Ltd.		554497403	manufacture(73252-133)