FDA.reportPublic FDA data

BLITZ RELIEF

Manufacturer
BLITZ PRODUCTS LLC
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:47:17

Label at a glance#

ProductBLITZ RELIEF
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure8 sections

Indications and uses

Temporary relief of minor muscle and joint pain associated with strains sprains cramps arthritis

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

CAMPHOR (4.0%)

MENTHOL (3.0%)

PURPOSE

OTC - PURPOSE SECTION

TOPICAL ANALGESIC

USES

INDICATIONS & USAGE SECTION

Temporary relief of minor muscle and joint pain associated with

  • strains
  • sprains
  • cramps
  • arthritis

WARNINGS

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Blitz_Pain Relief_2oz01b LBL_Blitz_Pain Relief_2oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2463934camphor 4 % / menthol 3 % Topical SprayPSN4
2463934camphor 40 MG/ML / menthol 30 MG/ML Topical SpraySCD4
2463934camphor 4 % / menthol 3 % Topical SpraySY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72676-101-112024-01-30C16284748780-11030e365-5329-111a-e063-dadaa90a10e2BLITZ RELIEF PAIN RELIEVING MUSCLE RUB (72676-101)
72676-101-122024-01-30C16284748780-11030e365-5329-111a-e063-dadaa90a10e2BLITZ RELIEF PAIN RELIEVING MUSCLE RUB (72676-101)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72676-101-11BLITZ RELIEF29.57 mL in 1 BOTTLE, SPRAYSPRAY29.574
72676-101-12BLITZ RELIEF59 mL in 1 BOTTLE, SPRAYSPRAY594

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72676-101BLITZ RELIEF (CAMPHOR, MENTHOL) SPRAY [BLITZ PRODUCTS LLC]4Legacy NDC, 2 package rows20220121_07db901c-8985-4700-b438-ac5fbb982947.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72676-10172676-101-12, 72676-101-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
1,2-HEXANEDIOLTR046Y3K1GIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
LAVENDER OILZBP1YXW0H8IACT
MAGNESIUM CHLORIDE02F3473H9OIACT
PEPPERMINT OILAV092KU4JHIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
PEG-100 STEARATEYD01N1999RIACT
PROPANEDIOL5965N8W85TIACT
ROSEMARY OIL8LGU7VM393IACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
MENTHOLL7T10EIP3AACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d607ac71-c00e-9d76-e053-2a95a90a210d07db901c-8985-4700-b438-ac5fbb9829472022-01-20WarningsExact identifier
spl id: d607ac71-c00e-9d76-e053-2a95a90a210d
spl set id: 07db901c-8985-4700-b438-ac5fbb982947

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.