EXTRA STRENGTH NATURALLY HL SUNBURN RELIEF- lidocaine hcl liquid

extra strength naturally hl sunburn relief by

Drug Labeling and Warnings

extra strength naturally hl 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 NATURALLY HL SUNBURN RELIEF 
lidocaine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69804-040
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
NUTMEG OIL (UNII: Z1CLM48948)	75 mg  in 1000 mg
PIPER METHYSTICUM WHOLE (UNII: 3P306S300W)	200 mg  in 1000 mg
ACHILLEA MILLEFOLIUM OIL (UNII: 97P5D0WG43)	75 mg  in 1000 mg
WITCH HAZEL (UNII: 101I4J0U34)	510 mg  in 1000 mg
COPAIBA OIL (UNII: 64VX45Y68N)	100 mg  in 1000 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69804-040-08	14200 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/10/2017
2	NDC: 69804-040-07	28500 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/10/2017
3	NDC: 69804-040-04	113400 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/10/2017
4	NDC: 69804-040-01	56700 mg in 1 BOTTLE, SPRAY; 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(69804-040)