BLITZ RELIEF- camphor, menthol spray

BLITZ RELIEF by

Drug Labeling and Warnings

BLITZ RELIEF by is a Otc medication manufactured, distributed, or labeled by BLITZ PRODUCTS LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

CAMPHOR (4.0%)

MENTHOL (3.0%)

PURPOSE

TOPICAL ANALGESIC

USES

Temporary relief of minor muscle and joint pain associated with

• strains
• sprains
• cramps
• arthritis

WARNINGS

For external use only

When using this product: use only as directed

• do not bandage tightly or use with a heating pad
• avoid contact with eyes or mucus membrane
• don’t apply to wounds or damaged skin
• wash hands after use with cold water

Stop use and ask a doctor if:

• condition worsens
• symptoms persist for more than 7 days or clear up and occur again within a few days
• redness is present
• irritation develops

If pregnant or breast-feeding: Ask a health professional before use

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children: If accidentally ingested, get medical help or contact a Poison Control Center immediately

DIRECTIONS

Adults and children 10 years of age and older:

• shake before using
• spray generously to affected areas
• massage thoroughly to receive maximum benefit
• not more than 4 times a day

INACTIVE INGREDIENTS

1, 2-Hexanediol, Arnica Montana Flower Extract, Butylene Glycol, Calendula Officinalis Flower Extract, Caprylyl Glycol, Fragrance, Glycerin, Glyceryl Stearate, Hydroxylethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Lavandula Angustifolia (Lavender) Oil, Magnesium Chloride, Mentha Arvensis (Peppermint) Leaf Oil, PEG-40 Hydrogenated Castor Oil, PEG-100 Stearate, Propanediol, Rosmarinus Officinalis (Rosemary) Leaf Oil, SD Alcohol 40, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BLITZ RELIEF 
camphor, menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72676-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	3 g  in 100 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
LAVENDER OIL (UNII: ZBP1YXW0H8)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
PEPPERMINT OIL (UNII: AV092KU4JH)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
PEG-100 STEARATE (UNII: YD01N1999R)
PROPANEDIOL (UNII: 5965N8W85T)
ROSEMARY OIL (UNII: 8LGU7VM393)
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72676-101-12	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/13/2020
2	NDC: 72676-101-11	29.57 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/13/2020

Labeler - BLITZ PRODUCTS LLC (116765479)