EXTRA STRENGTH SUNBURN RELIEF- lidocaine hcl cream

extra strength sunburn relief by

Drug Labeling and Warnings

extra strength sunburn relief by is a Otc medication manufactured, distributed, or labeled by ridge properties. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

WARNINGS

KEEP OUT OF REACH OF CHILDREN

PURPOSE

INDICATIONS & USAGE

ACTIVE INGREDIENT

INACTIVE INGREDIENT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EXTRA STRENGTH SUNBURN RELIEF 
lidocaine hcl cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69804-039
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	40 mg  in 1000 mg

Inactive Ingredients
Ingredient Name	Strength
PROPOLIS WAX (UNII: 6Y8XYV2NOF)	40 mg  in 1000 mg
PIPER METHYSTICUM WHOLE (UNII: 3P306S300W)	190 mg  in 1000 mg
WITCH HAZEL (UNII: 101I4J0U34)	400 mg  in 1000 mg
COPAIBA OIL (UNII: 64VX45Y68N)	90 mg  in 1000 mg
NUTMEG OIL (UNII: Z1CLM48948)	60 mg  in 1000 mg
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)	120 mg  in 1000 mg
ACHILLEA MILLEFOLIUM OIL (UNII: 97P5D0WG43)	60 mg  in 1000 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69804-039-06	14200 mg in 1 JAR; Type 0: Not a Combination Product	02/10/2017
2	NDC: 69804-039-05	28500 mg in 1 JAR; Type 0: Not a Combination Product	02/10/2017
3	NDC: 69804-039-02	56700 mg in 1 JAR; Type 0: Not a Combination Product	02/10/2017
4	NDC: 69804-039-03	113400 mg in 1 JAR; Type 0: Not a Combination Product	02/10/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/10/2017

Labeler - ridge properties (029478762)

Establishment
Name	Address	ID/FEI	Business Operations
ridge properties		029478762	manufacture(69804-039)