Ubre Mastitis Ointment

Ubre Mastitis Ointment
SPL v5
SPL
SPL Set ID bfc83a7d-49ed-d1e0-e053-2a95a90acf36
Route
TOPICAL
Published
Effective Date 2021-03-29
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Salicylic Acid (20 mg)
Inactive Ingredients
White Petrolatum D&c Brown No. 1 Lanolin Oil Camphor (synthetic) Ichthammol

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2019-03-29

Description

Methyl Salicylate 2%

Purpose

Topical Analgesic


Medication Information

Indications and Usage

Do not use, if prone to allergic reaction from any of the ingredients.

Do not use n on children • on irritated skin • in or near eyes or mucous membranes • on wounds or damaged skin.

Purpose

Topical Analgesic

Description

Methyl Salicylate 2%

Uses

Temporary relief of minor pain n joint & muscular aches n strains & sprain n backache.

Section 50569-3

Stop use and ask a doctor n if condition worsens or cleans up and occurs again n if symptoms persist for more than 7 days or irritation or severe burning occurs.

Section 51945-4

Section 53414-9

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

Warnings

For external use only

Do not use on large areas of the body. • if you are taking any other medication or drinking alcohol • if safety seal is torn, broken or missing.

Directions

Adults and children 12 years and older; apply to the affected area • no more than 3 to 4 times daily n children under 12 years of age; ask a Doctor.

Active Ingredient

Methyl Salicylate 2%

Other Information

Store at controlled room temperature 15-30ºC (59-86ºF)

Inactive Ingredients

Camphor crystals, D&C Brown #1, Lanolin, Ichthammol, and white petrolatum.


Structured Label Content

Uses

Temporary relief of minor pain n joint & muscular aches n strains & sprain n backache.

Indications and Usage (34067-9)

Do not use, if prone to allergic reaction from any of the ingredients.

Do not use n on children • on irritated skin • in or near eyes or mucous membranes • on wounds or damaged skin.

Section 50569-3 (50569-3)

Stop use and ask a doctor n if condition worsens or cleans up and occurs again n if symptoms persist for more than 7 days or irritation or severe burning occurs.

Section 51945-4 (51945-4)

Section 53414-9 (53414-9)

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

Purpose

Topical Analgesic

Warnings

For external use only

Do not use on large areas of the body. • if you are taking any other medication or drinking alcohol • if safety seal is torn, broken or missing.

Directions

Adults and children 12 years and older; apply to the affected area • no more than 3 to 4 times daily n children under 12 years of age; ask a Doctor.

Active Ingredient

Methyl Salicylate 2%

Other Information

Store at controlled room temperature 15-30ºC (59-86ºF)

Inactive Ingredients

Camphor crystals, D&C Brown #1, Lanolin, Ichthammol, and white petrolatum.


Advanced Ingredient Data


Raw Label Data

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