Meijer Medicated Cold and Hot Pain Relieving
- Manufacturer
- Sklar BOV Solutions Inc
- Effective date
- 2022-01-31
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:47:49
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Use
Temporarly releaves minor aches and pains of muscles and joints associated wotj artjrotos, , simple backaches, strains, bruses,
and sprains
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient Purpose
Menthol 16% Topical Analgesic
WARNINGS SECTION
Warnings
For external use only
Flammable
Keep away for from fire or flame. Do not puncture or incinerate.
Contents under pressure. Do not store at temperatures above 120ºF.
INDICATIONS & USAGE SECTION
When using this product, avoid contact with eyes and mucouse membranes.
Do not apply to wounds or damaged skin
Do not bandage tightly
Use only as directed
Stop use and ask a doctor if condition worsens, symptoms presist for more than 7 days, or clears up and occur again within
a few days.
needed for more that a weekl
If pregnant or breastfeeding ask a health professional before use.
DOSAGE & ADMINISTRATION SECTION
Directions , Adults and Children over 12 years old
Spray affected area with desired amount of product,
Repeat at needed but no more that 3 - 4 times dailiy
Children 12 years of younger.
Consult a physician
INACTIVE INGREDIENT SECTION
Inactive Ingredients
Alcohol denat. glycerin, propylene glycol, water
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep our of reach of Children. If ingested get medical help or contact a Poison Control Center immediatly
OTC - QUESTIONS SECTION
Questions 1-800-255-3924
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
113 g NDC52313-1110 Meijer Medicated Cold & Hot Pain Relieving
Menthol 16%
Quick Drying | Vanishing Scent
Non-Greasy
Sprays at any angle
Pain Relief Therapy for
Arthritis, Backache
Muscle Strains and Springs
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52313-1110-1 | 2024-01-30 | C162847 | 48780-1 | d6a99b39-3c91-a426-e053-dadaa90af4c2 | Meijer Medicated Cp;d amd hot Pain Relieving |
| 52313-1110-1 | 2022-01-31 | C162847 | 48780-1 | d6a99b39-3c91-a426-e053-dadaa90af4c2 | Meijer Medicated Cp;d amd hot Pain Relieving |
| 52313-1110-1 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-3c91-a426-e053-dadaa90af4c2 | Meijer Medicated Cp;d amd hot Pain Relieving |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52313-1110-1 | Meijer Medicated Cold and Hot Pain Relieving | 113 g in 1 CAN | SPRAY | 113 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52313-1110 | MEIJER MEDICATED COLD AND HOT PAIN RELIEVING (COLD AND HOT) SPRAY [SKLAR BOV SOLUTIONS INC] | 2 | Legacy NDC, 1 package rows | 20220201_a4eac137-08b5-50f2-e053-2a95a90a89fa.zip |
Products#
Every source-derived product name is available through these pages.
- Meijer Medicated Cold and Hot Pain Relieving
- Cold and Hot
- WATER
- ALCOHOL
- GLYCERIN
- MENTHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 52313-1110 | 52313-1110-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| d6e77490-e2f3-2c22-e053-2a95a90ae02a | a4eac137-08b5-50f2-e053-2a95a90a89fa | 2022-01-31 | Warnings | d6e77490-e2f3-2c22-e053-2a95a90ae02a a4eac137-08b5-50f2-e053-2a95a90a89fa |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
