LubeLife Climax Control Delay
- Product NDC
- 71683-005
- 11-digit product format
- 716830005
- Labeler code
- 71683
- Product ID
- 71683-005_3e62265a-9563-8fee-e063-6394a90a13d4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- CC Wellness LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-01-01
- Substance
- BENZOCAINE
- Active strength
- 7.5 g/100mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LubeLife Climax Control Delay
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 7.5 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71683-005-01 | LubeLife Climax Control Delay | 1 in 1 BOX | SPRAY | 1 | | 3 |
| 71683-005-02 | LubeLife Climax Control Delay | 60 mL in 1 BOTTLE, PLASTIC | SPRAY | 60 | | 3 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71683-005-01 | 71683000501 | 1 BOTTLE, PLASTIC in 1 BOX (71683-005-01) / 60 mL in 1 BOTTLE, PLASTIC (71683-005-02) | | 2022-01-01 | 0000-00-00 | No | No | Current |
| 71683-005-02 | 71683000502 | 60 mL in 1 BOTTLE, PLASTIC | 60 ml | | | | | Historical |