GERMA CAMPHOR ANALGESIC- camphor 10% ointment

Germa Camphor by

Drug Labeling and Warnings

Germa Camphor by is a Otc medication manufactured, distributed, or labeled by Germa Products, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Camphor 10%

Uses

Temporary relief of minor pain Rheumatism Muscular aches Arthritis Backache

INDICATIONS & USAGE

Do not use on children on irritated skin in or near eyes or mucous membranes on wounds or damaged skin if prone to allergic reaction from any of the ingredient on large areas of the body. if you are taking any other medication or drinking alcohol if safety seal is torn, broken or missing.

Purpose

Topical Analgesic

Warnings

For external use only

Do not use on children on irritated skin in or near eyes or mucous membranes on wounds or damaged skin if prone to allergic reaction from any of the ingredient on large areas of the body. if you are taking any other medication or drinking alcohol if safety seal is torn, broken or missing.

Warnings

KEEP OUT OF THE REACH OF CHILDREN

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding ask a health professional before use.

ASK DOCTOR

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

Other Information

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

Directions

Adults; 18 years of age and older, apply in affected area not more than 3 times daily.

Inactive Ingredients

Petrolatum

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GERMA CAMPHOR  ANALGESIC
camphor 10% ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73635-5809
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WHITE PETROLATUM (UNII: B6E5W8RQJ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73635-5809-2	56.69 mL in 1 JAR; Type 0: Not a Combination Product	03/29/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/29/2019

Labeler - Germa Products, LLC (116626935)